510(k) K822524
- Device
- EAR SPOON
- Applicant
- KELLEHER CORP.
- 510(k) number
- K822524
- Product code
- KBD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-09-09
- Date received
- 1982-08-23
- Regulation
- 874.4420
- Classification name
- Scissors, 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#
- 3006487092
- 9614069
- 8010769
- 9610612
- 3015398570
- 9680837
- 3014334038
- 8040884
- 9616250
- 9611616
- 2431166
- 3005809810
- 3036795921
- 3009255580
- 9680518
- 1052728
- 3009865268
- 3005067367
- 1421101
- 3015895045
- 9617426
- 3021680161
- 3005695838
- 3004608878
- 3003696170
- 3004001706
- 1032347
- 8010372
- 9611502
- 8010343
- 9710524
- 3011371465
- 1923569
- 3005061536
- 3010455030
- 9611112
- 9611503
- 1313525
- 9613083
- 1720747
- 2085947
- 3014201171
- 3013031133
- 8010851
- 8030607
- 8040881
- 2084346
- 3009513193
- 3013735167
- 9681622
- 2087382
- 8040263
- 3005440795
- 8040278
- 3013784566
- 8010235
- 1926681
- 3003644849
- 3008936260
- 3008338766
- 3003418325
- 1836161
- 1828464
- 1057946
- 3006554912
- 3033883491
- 3023657851
- 3003431869
- 3022862651
- 3004215117
- 3034688516
- 3029082594
- 2916714
- 3005528784
- 9611283
- 3016965929
- 8010386
- 1417592
- 9612278
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code KBD #
Legacy Summary#
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FDA Review#
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