CytoSoft

Non-sterile Cytology Brush CYB-100

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

Who Else Makes It

Concentrated in Shanghai (1), Jiangsu (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HHT
Manufacturer City Province Registered as Device types
Jiangsu Suyun Medical Materials Co., Ltd. Lianyungang Jiangsu Contract manufacturer 11
Shanghai NEO-Medical Import & Export Co., Ltd. Shanghai Shanghai Exporter 59
Ningbo HLS Medical Products Co., Ltd. Cixi Zhejiang Manufacturer 7

Record

Regulatory record for CytoSoft
Listed by Medical Packaging Corporation, United States
FDA product code HHT
Device type Spatula, Cervical, Cytological
Device class Class 2
Regulation 21 CFR 884.4530
Establishment Contract manufacturer, Manufacturer
510(k) K864323
Record published 2026-02-18

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for CytoSoft
Catalogue number Size Status
CYB-1 In distribution
CYB-100 In distribution
CSW-1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rovers® Cervex-Brush® Rovers Medical Devices B.V. 10
Andwin Scientific Andwin Scientific 9
Rovers® Cervex-Brush® Combi Rovers Medical Devices B.V. 8
Medscand Pap-Perfect Supply Tray Coopersurgical, Inc. 6
Papette Coopersurgical, Inc. 6
C20310 B & B Medical Technologies, Inc. 4
C27024 B & B Medical Technologies, Inc. 4
Cytobrush Plus GT Coopersurgical, Inc. 4
Rovers® EndoCervex-Brush® Rovers Medical Devices B.V. 4
C29000 B & B Medical Technologies, Inc. 4
Fisherbrand Fisher Scientific Company L.L.C. 4
Cytobrush Plus Coopersurgical, Inc. 4

Showing 12 of 49. All products under Spatula, Cervical, Cytological

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K870398 1987-02-25
K864323 1987-01-09

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