CIRCUMCISION KIT
FDA 510(k) clearance K770873 · decided 1977-07-11
Clearance details
- K-number
- K770873
- Device name
- CIRCUMCISION KIT
- Applicant
- American Hospital Supply Corp.
- Decision
- Substantially Equivalent
- Date received
- 1977-05-13
- Decision date
- 1977-07-11
- Days to decision
- 59 days
- Clearance type
- Traditional
- Product code
- FHG
- Device class
- 2
- Regulation number
- 884.4530
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705 (K911272) | Edward Weck, Inc. | 1991-07-02 |
Recalls involving this device
No recalls on record reference this clearance.