FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

PANAVIA SA CEMENT HANDMIX VALUE PACK (UNIVERSAL (A2), WHITE) PANAVIA SA CEMENT HANDMIX (UNIVERSAL (A2), WHITE) PANAVIA S

K Number: K120378 · Decision Mar 30, 2012
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
42
Review Days
52

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Basic Information

Device Name
PANAVIA SA CEMENT HANDMIX VALUE PACK (UNIVERSAL (A2), WHITE) PANAVIA SA CEMENT HANDMIX (UNIVERSAL (A2), WHITE) PANAVIA S
K Number
K120378
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kuraray Medical, Inc.
Date Received
February 7, 2012
Decision Date
March 30, 2012
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 Medical, Inc.

K Number Device Name
K120379 PANAVIA SA CEMENT AUTOMIX VALUE PACK (UNIVERSAL (A2), WHITE) PANAVIA SA CEMENT AUTOMIX (UNIVERSAL (A2), WHITE) PANAVIA S
K111975 CLEARFIL TRI-S BOND PLUS SINGLE DOSE STANDARD / VALUE / INTRODUCTORY PACK
K100328 CLEARFIL MAJETY POSTERIOR
K092281 CLEARFIL MAJESTY POSTERIOR PLT
K081583 CLEARFIL SA CEMENT
K071169 CLEARFIL MAJESTY POSTERIOR PLT
K070325 CLEARFIL MAJESTY ESTHETIC PLT
K062409 K-ETCHANT GEL
K061906 CLEARFIL CERAMIC PRIMER
K062382 CLEARFIL DC BOND
Search all 42 clearances from Kuraray Medical, Inc. →