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

PEFECT SHOT

K Number: K972019 · Decision Jul 3, 1997
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
281
Applicant Total
19
Review Days
32

Basic Information

Device Name
PEFECT SHOT
K Number
K972019
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
INTERNATIONAL IMAGING ELECTRONICS
Date Received
June 1, 1997
Decision Date
July 3, 1997
Product Code
EIA
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
EIA Unit, Operative Dental

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