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

VALULINE* AMALGAM ALLOY

K Number: K821971 · Decision Jul 20, 1982
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
73
Applicant Total
206
Review Days
14

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Basic Information

Device Name
VALULINE* AMALGAM ALLOY
K Number
K821971
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3070
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Johnson & Johnson Professionals, Inc.
Date Received
July 6, 1982
Decision Date
July 20, 1982
Product Code
EJJ
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
EJJ Alloy, Amalgam

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