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

PRECISION INTRA-ORAL SCOPES

K Number: K932878 · Decision Jan 6, 1994
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
13
Review Days
206

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Basic Information

Device Name
PRECISION INTRA-ORAL SCOPES
K Number
K932878
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Precise Optics
Date Received
June 14, 1993
Decision Date
January 6, 1994
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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K911744 PRECISION OPTICS CORPORATION LAPAROSCOPE
K903459 PRECISION OPTICS ENDOSCOPE ADAPTER
K903457 PRECISION OPTICS IMAGE BEAMSPLITTER (COUPLER)
K903458 PRECISION OPTICS IMAGE COUPLER
K820178 PI808 MOBILE C-ARM IMAGE INTENSIFIER
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