HCZClass II
Forceps, Surgical, Gynecological
21 CFR 884.4530 / Obstetrics/Gynecology
HCZ is the FDA product code for Forceps, Surgical, Gynecological, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold 24 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- HCZ
- Device name
- Forceps, Surgical, Gynecological
- Regulation
- 21 CFR 884.4530
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 24
- Ingested recalls
- 0
Clearances, product code HCZ
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1981 | 1 |
| 1983 | 1 |
| 1985 | 1 |
| 1989 | 6 |
| 1990 | 2 |
| 1991 | 1 |
| 1994 | 8 |
| 2009 | 1 |
| 2014 | 1 |
| 2018 | 1 |
Applicants with the most clearances
Product code HCZ| Applicant | Clearances |
|---|---|
| Thomasville Medical Assoc. | 6 |
| Kinetic Medical Products | 3 |
| Zinnanti Surgical Instruments, Inc. | 2 |
| Cook Incorporated | 1 |
| Cook, Inc. | 1 |
| Edward Weck, Inc. | 1 |
| Fetzer Medical GmbH & Co.KG | 1 |
| Imm Enterprises, Ltd. | 1 |
| Instrumed International Inc dba Avalign German Specialty Instruments | 1 |
| Integra LifeSciences Corporation | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.