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

ALASTIK

K Number: K940165 · Decision Mar 7, 1994
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
24
Applicant Total
23
Review Days
60

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Basic Information

Device Name
ALASTIK
K Number
K940165
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Unitek Corp.
Date Received
January 6, 1994
Decision Date
March 7, 1994
Product Code
ECI
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
ECI Band, Elastic, Orthodontic

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Other Clearances by Unitek Corp.

K Number Device Name
K944286 METAL-LINED TRANSCEND CERAMIC BRACKET
K933501 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
K880392 ORTHOLUX VISIBLE LIGHT CURING UNIT
Search all 23 clearances from Unitek Corp. →