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

CAVIDRY

K Number: K822896 · Decision Oct 22, 1982
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
30
Review Days
23

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Basic Information

Device Name
CAVIDRY
K Number
K822896
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Parker Laboratories, Inc.
Date Received
September 29, 1982
Decision Date
October 22, 1982
Product Code
EJH
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
EJH Alloy, Metal, Base

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