Histobrush
by Spectrum Co.
510(k) K874604
Histobrush is a medical device (FDA Class II; FDA product code HHT, Spatula, Cervical, Cytological) made by Spectrum Co., cleared under FDA 510(k) K874604 on 7 Jan 1988, active as of 10 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK874604 | Date7 Jan 1988 | StatusActive |
Official records
- FDA 510(k) database K874604
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HHT
- Device class
- Class II
- Regulation
- 21 CFR Part 884.4530
- Advisory committee
- Obstetrics/Gynecology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code HHT (Spatula, Cervical, Cytological).
- AMSINO CERVICAL SCRAPER by Amsino Intl., Inc.
- CELL COLLECTING BRUSH by Anderson Winn Paper Co.
- DIAMICS CERCOL CERVICAL SAMPLE COLLECTOR SYSTEM by Diamics, Inc.
- EOS BRAND DISPOSABLE CYTO/CERVICAL SAMPLER by NORTH EOS INDUSTRIES,INC.
- SPATULA, CERVICAL CYTOLOGICAL CYTOLOGY by Dyn-A-Med Products
- Puritan Histobrush 25-2199 by Puritan Medical Products Company
- CYTOSET(TM) by Birchwood Laboratories, Inc.
- ACCELLON CERVICAL BIOSAMPLER by Medscand AB
- ENDO C BRUSH by Milex Products, Inc.
- PAP SMEAR BRUSH by Donald G. Zeller