FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SILICONT BUR BLOCK

K Number: K921406 · Decision Apr 28, 1992
Classifications
1
FEI Numbers
264
Registration Numbers
264
Same Product Code
26
Applicant Total
6
Review Days
39

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Basic Information

Device Name
SILICONT BUR BLOCK
K Number
K921406
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3240
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Innovators, Inc.
Date Received
March 20, 1992
Decision Date
April 28, 1992
Product Code
EJL
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
EJL Bur, Dental

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K790984 KLIP-LITE