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

TEC-2110 GREEN LASER MODEL MT-HNG

K Number: K950293 · Decision Aug 18, 1995
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
27
Applicant Total
41
Review Days
205

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Basic Information

Device Name
TEC-2110 GREEN LASER MODEL MT-HNG
K Number
K950293
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.5780
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medtec, Inc.
Date Received
January 25, 1995
Decision Date
August 18, 1995
Product Code
IWE
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IWE Monitor, Patient Position, Light-Beam

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