ID NOW RSV

A rapid, automated, molecular test for the qualitative detection of respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal specimens.

Registry build 21.09.26
1manufacturer
1catalogue number
5510(k) clearances naming this product code

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OCC
Manufacturer City Province Registered as Device types
Hochuen Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 20

Record

Regulatory record for ID NOW RSV
Listed by Alere Scarborough, Inc., United States
FDA product code OCC
Device type Respiratory Virus Panel Nucleic Acid Assay System
Device class Class 2
Regulation 21 CFR 866.3980
510(k) K161375
Record published 2018-10-29
Record revised 2023-09-12 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for ID NOW RSV
Catalogue number Size Status
435-000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Panther Fusion® Hologic, Inc. 4
Prodesse Hologic, Inc. 4
Solana Diagnostic Hybrids, Inc. 2
Alere™ i Influenza A & B Control Swab Kit Alere Scarborough, Inc. 1
Silaris RSV Supplemental Pack Mesa Biotech, Inc. 1
Alere i RSV Control Swab Kit Alere Scarborough, Inc. 1
ID NOW Influenza A & B 2 Control Swab Kit Alere Scarborough, Inc. 1
Xpert Xpress Flu/RSV Cepheid 1
ID NOW Influenza A & B Control Swab Kit Alere Scarborough, Inc. 1
Simplexa™ Flu A/B & RSV Direct DiaSorin Molecular LLC 1
Alere™ i Influenza A & B Alere Scarborough, Inc. 1
Respiratory Virus Plus (RV+) Amplification Tray Nanosphere, Inc. 1

Showing 12 of 39. All products under Respiratory Virus Panel Nucleic Acid Assay System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173932 2018-01-26
K171792 2017-09-29
K163266 2016-12-21
K161375 2016-08-18
K151464 2015-07-28

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of ID NOW RSV
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Abbott Diagnostics Scarborough, Inc. 510(k) number 2025-03-04 Class II Process change control The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use. 178056 eaches (147472 US, 31584 OUS)
Abbott Diagnostics Scarborough, Inc. 510(k) number 2025-03-04 Class II Process change control the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use. 442,296 eaches

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