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

LUMENON XENON LIGHT SOURCE

K Number: K992050 · Decision Sep 14, 1999
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
46
Applicant Total
56
Review Days
89

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Basic Information

Device Name
LUMENON XENON LIGHT SOURCE
K Number
K992050
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Walter Lorenz Surgical, Inc.
Date Received
June 17, 1999
Decision Date
September 14, 1999
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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Other Clearances by Walter Lorenz Surgical, Inc.

K Number Device Name
K063386 LORENZ ORTHODONTIC ANCHORAGE SYSTEM
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K063506 LORENZ STERNAL CLOSURE SYSTEM
K062842 TWIST DRILL
K061384 LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM
K042516 OTOMIMIX
K030425 LORENZ RESORBABLE DISTRACTION SYSTEM OR EXPANDER
K040990 MODIFICATION TO SELF-DRILLING RADIOGRAPHIC MARKERS
K040983 LORENZ SELF-DRILLING IMF SCREW
K033740 LORENZ STERNAL CLOSURE SYSTEM
Search all 56 clearances from Walter Lorenz Surgical, Inc. →