FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DEBRACKETING INSTRUMENT

K Number: K924295 · Decision Nov 23, 1992
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
6
Applicant Total
23
Review Days
89

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Basic Information

Device Name
DEBRACKETING INSTRUMENT
K Number
K924295
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Unitek Corp.
Date Received
August 26, 1992
Decision Date
November 23, 1992
Product Code
JEX
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JEX Plier, Orthodontic

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K923432 GERMAN MINI DYNALOCK
K911271 ADHESIVE PRECOATED BRACKETS
K910288 NONSTAINING ALASTIKS
K890529 ALASTIGARD
K880392 ORTHOLUX VISIBLE LIGHT CURING UNIT
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