510(k) K891402
- Device
- UTERINE CLAMPS
- Applicant
- ZINNANTI SURGICAL INSTRUMENTS, INC.
- 510(k) number
- K891402
- Product code
- HGC
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1989-03-29
- Date received
- 1989-03-14
- Regulation
- 884.4520
- Classification name
- Clamp, Uterine
- Medical specialty
- Obstetrics/Gynecology
- Review panel
- Obstetrics/Gynecology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- ANNA STRAIGHT
- Address
- 21540-B Prairie St. Chatsworth CA US 91311 91311
FDA Registration Numbers#
- 3010055973
- 8010099
- 3008711893
- 8010422
- 3009134882
- 3010353847
- 3036795921
- 9616246
- 9616250
- 3008843439
- 1828464
- 3013358456
- 9612278
- 1421879
- 8043404
- 9610612
- 3006554912
- 3043355002
- 3005061536
- 8010697
- 3015972835
- 9613079
- 3011137372
- 3010699884
- 9611283
- 3014615697
- 3008936260
- 1421101
- 3005695838
- 9680718
- 3004215117
- 3010041511
- 8040278
- 1057946
- 2084346
- 9710524
- 3003431869
- 3029082594
- 3023620966
- 3005440795
- 9611112
- 3032747418
- 3016965929
- 3022862651
- 3008338766
- 3002834291
- 3007137643
- 3010687973
- 3008902714
- 1836161
- 9610905
- 3001620590
- 8040233
- 3005067367
- 3031564283
- 1056350
- 3008797953
- 3015895045
- 3008770252
- 3007648354
- 3005528784
- 2916714
- 2431166
- 3003244954
- 9680518
- 9614062
- 9612086
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HGC #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K771344 | GUSBERG HYSTERECTOMY CLAMP | J. Sklar Mfg. Co., Inc. | 1977-07-27 |
Legacy Summary#
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FDA Review#
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