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

FUTURA GLASS IONOMER SILVER REINFORCED

K Number: K991974 · Decision Sep 17, 1999
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
13
Review Days
98

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Basic Information

Device Name
FUTURA GLASS IONOMER SILVER REINFORCED
K Number
K991974
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ab Ardent
Date Received
June 11, 1999
Decision Date
September 17, 1999
Product Code
EMA
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
EMA Cement, Dental

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Other Clearances by Ab Ardent

K Number Device Name
K131753 MERIDIAN
K040465 LATIT FLOW
K022971 MICROHYBRID 11
K022973 ADHESIVE 14
K022972 MICROFILL 13
K022974 MICROHYBRID 12
K022975 ETCHING 15
K020452 HIGH SILVER CONVENTIONAL
K011801 FUTURA TOPCAP NON GAMMA-2
K982458 VIVALLOY HR
Search all 13 clearances from Ab Ardent →