FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ORTHODONITC METAL REINFORCED PLASTIC BRACKET

K Number: K942826 · Decision Dec 14, 1994
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
41
Applicant Total
13
Review Days
183

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Basic Information

Device Name
ORTHODONITC METAL REINFORCED PLASTIC BRACKET
K Number
K942826
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gac Intl., Inc.
Date Received
June 14, 1994
Decision Date
December 14, 1994
Product Code
DYW
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
DYW Bracket, Plastic, Orthodontic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYW), ordered by most recent decision date.

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Other Clearances by Gac Intl., Inc.

K Number Device Name
K981036 SMARTBOND
K933542 MESIAL LOOP BAR
K932825 MICROARCH GOLD BRACKET
K932319 ORTHODONTIC ELASTOMER
K932025 ION-IMPLANTED NEO SENTALLOY
K920905 BIOFORCE WIRE
K923029 ORTHODONTIC STAINLESS STEEL BRACKET
K920850 GAC THUMB-SUCKING CONTROL APPLIANCE
K920784 ORTHODONTIC FACE BOW W/ INNER WIRE
K852179 CERAMIC ORTHODONIT APPLIANCE
Search all 13 clearances from Gac Intl., Inc. →