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

GAC THUMB-SUCKING CONTROL APPLIANCE

K Number: K920850 · Decision Aug 24, 1992
Classifications
1
FEI Numbers
168
Registration Numbers
168
Same Product Code
29
Applicant Total
13
Review Days
181

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Basic Information

Device Name
GAC THUMB-SUCKING CONTROL APPLIANCE
K Number
K920850
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gac Intl., Inc.
Date Received
February 25, 1992
Decision Date
August 24, 1992
Product Code
DZC
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
DZC Wire, Orthodontic

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Other Clearances by Gac Intl., Inc.

K Number Device Name
K981036 SMARTBOND
K942826 ORTHODONITC METAL REINFORCED PLASTIC BRACKET
K933542 MESIAL LOOP BAR
K932825 MICROARCH GOLD BRACKET
K932319 ORTHODONTIC ELASTOMER
K932025 ION-IMPLANTED NEO SENTALLOY
K920905 BIOFORCE WIRE
K923029 ORTHODONTIC STAINLESS STEEL BRACKET
K920784 ORTHODONTIC FACE BOW W/ INNER WIRE
K852179 CERAMIC ORTHODONIT APPLIANCE
Search all 13 clearances from Gac Intl., Inc. →