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

LINER, CAVITY CALCIUM HYDROXIDE

K Number: K781688 · Decision Dec 20, 1978
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
32
Review Days
77

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Basic Information

Device Name
LINER, CAVITY CALCIUM HYDROXIDE
K Number
K781688
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3250
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Kerr Corporation (Danbury)
Date Received
October 4, 1978
Decision Date
December 20, 1978
Product Code
EJK
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
EJK Liner, Cavity, Calcium Hydroxide

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