510(k) K791121
- Device
- ALLIGATOR FORECPTS, CUPPED FORCEPS
- Applicant
- XOMED, INC.
- 510(k) number
- K791121
- Product code
- JYR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-06-27
- Date received
- 1979-06-15
- Regulation
- 874.4420
- Classification name
- Nipper, Malleus
- Medical specialty
- Ear Nose & Throat
- Review panel
- Ear Nose & Throat
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 1318 Lonedell Rd. Arnold MO US 63010 63010
FDA Registration Numbers#
- 8030607
- 3004608878
- 9613926
- 8010422
- 1417592
- 3016825318
- 3010353847
- 3036795921
- 8010168
- 3035678069
- 3012995405
- 3002858762
- 3013358456
- 1421879
- 3014680812
- 9680837
- 3006554912
- 3012494290
- 3005809810
- 3005092287
- 8010282
- 3043226252
- 1932180
- 3011137372
- 8010528
- 3011625373
- 9681129
- 3014615697
- 3008936260
- 9611283
- 1421101
- 1926681
- 2529846
- 3004215117
- 3012507533
- 3010041511
- 3003418325
- 8040278
- 1057946
- 2084346
- 1055890
- 9710524
- 9612074
- 3006487092
- 8010395
- 9611112
- 3003759558
- 3002807115
- 3008338766
- 3002834291
- 8043752
- 1313525
- 1836161
- 1923569
- 9610905
- 9615004
- 8040233
- 3005067367
- 3014334038
- 9611367
- 3004001706
- 9610612
- 3008770252
- 3005528784
- 2916714
- 3003244954
- 9611503
- 8043496
- 3009513193
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code JYR #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K822170 | INCUS NIPPERS | Kelleher Corp. | 1982-08-24 |
Legacy Summary#
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FDA Review#
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