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

GTI CLASP COVER

K Number: K913200 · Decision Feb 3, 1992
Classifications
1
FEI Numbers
205
Registration Numbers
205
Same Product Code
913
Applicant Total
2
Review Days
201

Basic Information

Device Name
GTI CLASP COVER
K Number
K913200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GTI, INC.
Date Received
July 17, 1991
Decision Date
February 3, 1992
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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K Number Device Name
K860347 SUNLAMP MODELS 24N, 30R, 30RE, 37RE