Nova

NOVA 1/1+ Analyzer w/ Printer (No Acc Pack)

Registry build 21.09.26
2manufacturers in China registered for this device type
6catalogue numbers in this listing
21510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code JGS
Manufacturer City Province Registered as Device types
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Record

Regulatory record for Nova
Listed by Nova Biomedical Corporation, United States
FDA product code JGS
Device type Electrode, Ion Specific, Sodium
Device class Class 2
Regulation 21 CFR 862.1665
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K963005
Record published 2016-09-20
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number
Storage Handling environment temperature 15 to 30 °C; Storage environment temperature 15 to 30 °C
Packaging Carton, box

Catalogue Numbers

Catalogue numbers for Nova
Catalogue number Size Status
16 In distribution
1 In distribution
1 In distribution
10 In distribution
1/4/5/8/10/11/12/13/14 In distribution
8 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stat Profile Nova Biomedical Corporation 13
i-STAT Abbott Point OF Care Inc. 9
AU Beckman Coulter, Inc. 8
GEM Premier ChemSTAT PAK Na+,K+,Ca++,Cl-, Glu, Crea, BUN, tCO2, Hct, Lac,pH,pCO2 Instrumentation Laboratory SPA 8
Phoenix Diagnostics, Inc. Phoenix Diagnostics, Inc. 5
Sodium Electrode Roche Diagnostics Gmbh 4
Pointe Scientific, Inc. Horiba Instruments Incorporated 3
Architect Abbott Laboratories 3
Synermed® Infrared Laboratory Systems LLC 3
Sodium Electrode Diamond Diagnostics Inc. 3
Phoenix Diagnostics Phoenix Diagnostics, Inc. 2
Sodium Electrode Medica Corp. 2

Showing 12 of 88. All products under Electrode, Ion Specific, Sodium

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K200403 2020-04-14
K191365 2019-07-19
K180428 2018-08-15
K001761 2000-08-07
K000895 2000-04-17
K924547 1993-01-28
K923806 1992-09-29
K921937 1992-07-27
K922215 1992-07-17
K915176 1992-01-15
K912560 1991-07-17
K912559 1991-07-01
K905264 1991-03-05
K894218 1989-09-07
K880750 1988-07-01
K881255 1988-05-16
K874832 1988-02-11
K872190 1987-06-24
K811289 1981-05-27
K801882 1980-09-16
K770601 1977-06-14

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2023-09-18 Class II Process design Potential risk of reporting erroneous creatinine patient results associated with the initial start-up of a new BUN/Creatinine Sensor Cartridge. The potential risk is within the first 2-4 hours after cartridge installation that may not be id 161 units
2023-09-18 Class II Process design Potential risk of reporting erroneous creatinine patient results associated with the initial start-up of a new BUN/Creatinine Sensor Cartridge. The potential risk is within the first 2-4 hours after cartridge installation that may not be id 1779 units: 438 US; 1341 OUS

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer