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

WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT

K Number: K951519 · Decision Jun 14, 1995
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
1
Applicant Total
15
Review Days
72

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Basic Information

Device Name
WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT
K Number
K951519
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4160
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Wells Johnson Co.
Date Received
April 3, 1995
Decision Date
June 14, 1995
Product Code
FWL
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FWL Camera, Cine, Endoscopic, Without Audio

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K945500 WELLS JOHNSON FIXATION SYSTEM
K945877 WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT
K945805 WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE
K854068 EXTERNAL MECHANICAL FASTENER
K843188 WELLS JOHNSON CO. CHAJ-CHIR-SUCTION TIP
K832520 SUCTION TIPS
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