510(k) K781837
- Device
- Wound Span Bridge Iii
- Applicant
- HOWMEDICA CORP.
- 510(k) number
- K781837
- Product code
- KAS
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-11-15
- Date received
- 1978-10-30
- Regulation
- 874.4420
- Classification name
- Knife, Nasal
- Medical specialty
- Ear, Nose, Throat
- Review panel
- Ear, Nose, Throat
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3023657851
- 9611112
- 3005440795
- 3004215117
- 2249529
- 2431166
- 9615857
- 1421879
- 8040278
- 8010099
- 3010041511
- 1923569
- 3014615697
- 9611283
- 9613926
- 1313525
- 3003244954
- 8043816
- 3015895045
- 3008808049
- 3002862271
- 3015972835
- 1032347
- 3001620590
- 3015451162
- 1836161
- 3029082594
- 9680837
- 2529846
- 8044098
- 9616246
- 2434839
- 3003418325
- 1828464
- 2085947
- 3013497507
- 3011137372
- 1646747
- 3010202439
- 3007137643
- 1417592
- 8040233
- 2916714
- 9613083
- 1057946
- 9612074
- 9680519
- 9613079
- 3006897996
- 3005528784
- 9610612
- 3036795921
- 3014334038
- 1932180
- 3008936260
- 3005809810
- 9710524
- 3005067367
- 3006554912
- 2020550
- 9615004
- 3008770252
- 9612075
- 9680518
- 9617426
- 1926681
- 3034688516
- 3004608878
- 1421101
- 9610905
- 3012995405
- 8030607
- 1720747
- 1052728
- 8010433
- 3022862651
- 3005061536
- 9680718
- 3016965929
Source Documents#
510(k) summary PDF not indicated by FDA