Vaportrode Vaporization Electrode -Grooved/Fluted/Spiked(Gve-B, Gve-F, Gve-S) & Vaportomme Vaporization Loop (Gve-Lg)
by Circon Corp.
510(k) K964594
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK964594 | Date15 Aug 1997 | StatusActive |
Recalls
No FDA recalls found in the data synced 11 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- KNF
- Device Class
- Class II
- Regulation
- 21 CFR Part 884.4160
- Advisory Committee
- Obstetrics/Gynecology
- FDA Decision
- SESE Substantially Equivalent