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

MODIFICATION TO PANAVIA F

K Number: K002322 · Decision Sep 18, 2000
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
11
Review Days
49

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Basic Information

Device Name
MODIFICATION TO PANAVIA F
K Number
K002322
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kuraray America, Inc.
Date Received
July 31, 2000
Decision Date
September 18, 2000
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 Kuraray America, Inc.

K Number Device Name
K111982 CLEARFIL DC CORE PLUS
K111980 CLEARFIL TRI-S BOND PLUS
K063595 CLEARFIL MAJESTY POSTERIOR
K063593 CLEARFIL MAJESTY FLOW
K063228 SURFACE COAT
K983361 PANAVIA F
K982259 CHROMA ZONE COLOR STAIN
K982164 ESTENIA
K974486 CLEARFIL LINER BOND 2V
K974089 ALLOY PRIMER
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