FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CONMED LINVATEC 300W XENON LIGHT SOURCE

K Number: K070376 · Decision Aug 20, 2007
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
46
Applicant Total
21
Review Days
193

Basic Information

Device Name
CONMED LINVATEC 300W XENON LIGHT SOURCE
K Number
K070376
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CONMED LINVATEC
Date Received
February 8, 2007
Decision Date
August 20, 2007
Product Code
GCT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
GCT Light Source, Endoscope, Xenon Arc

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K101100 CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503
K092898 CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES
K090560 CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS
K083161 ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)
K080531 CONMED LINVATEC MICROFRACTURE INSTRUMENT STERILIZATION TRAY
K072291 CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR
K080444 CONMED LINVATEC OSPREY DRILL SYSTEM
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