Rocket Cervical Spatula
510(k) K884042
Rocket Cervical Spatula 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) K884042 on 7 Oct 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 | NumberK884042 | Date7 Oct 1988 | StatusActive |
Official records
- FDA 510(k) database K884042
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- Withdrawn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
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