Acurrett®

Catalogue number Accurett 8G, listed by H&O Equipments, Nv/Sa, Belgium, under Unit, Cryosurgical, Accessories. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (1), Beijing (1), Tianjin (1).

Chinese manufacturers registered for FDA product code GEH
Manufacturer City Province Registered as Device types
Shenzhen Kesite Digital Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Hygea Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2
Medinux (Tianjin) Technologies Co., Ltd. Tianjin Tianjin Manufacturer 1

Record

Regulatory record for Acurrett®
Listed by H&O Equipments, Nv/Sa, Belgium
FDA product code GEH
Device type Unit, Cryosurgical, Accessories
Device class Class 2
Regulation 21 CFR 878.4350
510(k) K161615
Record published 2018-02-06
Record revised 2021-04-07 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for Acurrett®
Catalogue number Size Status
Accurett 8G In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Frigitronics Coopersurgical, Inc. 42
CryoProbe™ H&O Equipments, Nv/Sa 35
Wallach Coopersurgical, Inc. 32
Premier Premier Dental Products Co. 30
Hygea Hygea Medical Technology Co., Ltd. 26
truFreeze CSA Medical 20
Freezpen® H&O Equipments, Nv/Sa 19
Leisegang Cryotip for LM-900 Coopersurgical, Inc. 15
Integra® Miltex® Integra LifeSciences Production Corporation 13
cryoICE Cryoablation System Atricure, Inc. 13
CryoThin Medinux (Tianjin) Technologies Co., Ltd. 12
Erbe Erbe Elektromedizin GmbH 12

Showing 12 of 334. All products under Unit, Cryosurgical, Accessories

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K161615 2016-08-23
K024009 2003-03-20

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