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

MESIAL LOOP BAR

K Number: K933542 · Decision Aug 5, 1994
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
6
Applicant Total
13
Review Days
381

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Basic Information

Device Name
MESIAL LOOP BAR
K Number
K933542
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
July 20, 1993
Decision Date
August 5, 1994
Product Code
ECO
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
ECO Spring, Orthodontic

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Other Clearances by Gac Intl., Inc.

K Number Device Name
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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
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