Rocket Endocervical Brush
510(k) K885274
Rocket Endocervical Brush is a medical device (FDA Class II; FDA product code HHT, Spatula, Cervical, Cytological) made by A & A Medical, Inc., cleared under FDA 510(k) K885274 on 9 Mar 1989, active as of 11 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 | NumberK885274 | Date9 Mar 1989 | StatusActive |
Official records
- FDA 510(k) database K885274
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- Withdrawn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).
- PAP-PAK CYTOBRUSH KIT by Medical Packaging Corporation
- CERVEX-BRUSH by Unimar, Inc.
- DETECT (TM) CYTOLOGY BRUSH by Cook Ob/Gyn
- SAFETEX CHLAMYDIA TRACHOMATIS SPECIMEN COLLECTION KIT by Andwin Scientific
- CERVICAL BRUSH by Statlab Medical Products, Inc.
- Puritan Histobrush® 25-2188 by Puritan Medical Products Company
- C-E BRUSH by Surgipath Medical Industries, Inc.
- Puritan Histobrush Cytology Brush 2199 by Puritan Medical Products Company
- CERVEX-BRUSH PAP KIT by Rovers Diagnostic Devices
- BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGY by Bio Nuclear Diagnostics Inc