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KBQ

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Knife, Tonsil
Device class
Class I (low risk)
Regulation
21 CFR 874.4420
Medical specialty
Ear, Nose, Throat
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RecordFirmDate
TONSIL KNIFE-VARIOUS (K841005)Premier Dental Products Co.1984-05-30

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