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

PANAVIA 21

K Number: K933030 · Decision Feb 24, 1994
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
25
Review Days
247

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Basic Information

Device Name
PANAVIA 21
K Number
K933030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kuraray Co.
Date Received
June 22, 1993
Decision Date
February 24, 1994
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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