510(k) K841005
- Device
- TONSIL KNIFE-VARIOUS
- Applicant
- PREMIER DENTAL PRODUCTS CO.
- 510(k) number
- K841005
- Product code
- KBQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-05-30
- Date received
- 1984-03-09
- Regulation
- 874.4420
- Classification name
- Knife, Tonsil
- 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#
- 8010099
- 8030607
- 3004608878
- 9613926
- 3003435550
- 3023657851
- 1417592
- 3013784566
- 3002862271
- 3006897996
- 8043816
- 1421879
- 3013497507
- 8044098
- 9680837
- 3006554912
- 3005809810
- 3015972835
- 1932180
- 3015451162
- 3011137372
- 9680519
- 9611283
- 1421101
- 1926681
- 2529846
- 3010041511
- 3003418325
- 8040278
- 1055890
- 8010704
- 9611112
- 3016965929
- 3001408183
- 3007137643
- 1313525
- 9612075
- 1836161
- 1923569
- 3002976036
- 9610612
- 3005067367
- 3014334038
- 3005528784
- 3008770252
- 2916714
- 9613083
- 9680518
- 8043496
- 3009513193
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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