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

UNITEK DISPOSABLE IMPRESSION SYRINGE

K Number: K851386 · Decision Apr 29, 1985
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
12
Applicant Total
23
Review Days
20

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Basic Information

Device Name
UNITEK DISPOSABLE IMPRESSION SYRINGE
K Number
K851386
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Unitek Corp.
Date Received
April 9, 1985
Decision Date
April 29, 1985
Product Code
EID
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
EID Syringe, Restorative And Impression Material

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Other Clearances by Unitek Corp.

K Number Device Name
K944286 METAL-LINED TRANSCEND CERAMIC BRACKET
K933501 ALASTIK
K940165 ALASTIK
K923999 ALASTIK NS
K924645 TRANSCEND SERIES 6000 DEBONDING INSTRUMENTS
K924295 DEBRACKETING INSTRUMENT
K923432 GERMAN MINI DYNALOCK
K911271 ADHESIVE PRECOATED BRACKETS
K910288 NONSTAINING ALASTIKS
K890529 ALASTIGARD
Search all 23 clearances from Unitek Corp. →