510(k) K770873
- Device
- CIRCUMCISION KIT
- Applicant
- American Hospital Supply Corp.
- 510(k) number
- K770873
- Product code
- FHG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-07-11
- Date received
- 1977-05-13
- Regulation
- 884.4530
- Classification name
- Bell, Circumcision
- Medical specialty
- Obstetrics/Gynecology
- Review panel
- Obstetrics/Gynecology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 1836161
- 9612278
- 3018071447
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FHG#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K911272 | ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705 | Edward Weck, Inc. | 1991-07-02 |