Atlas FDA

ENDOSCOPIC LIGHT SOURCE XL202/L3

FDA 510(k) clearance K020889 · decided 2002-06-05

Clearance details

K-number
K020889
Device name
ENDOSCOPIC LIGHT SOURCE XL202/L3
Applicant
World of Medicine Lemke GmbH
Decision
Substantially Equivalent
Date received
2002-03-19
Decision date
2002-06-05
Days to decision
78 days
Clearance type
Traditional
Product code
GCT
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Cambridge, MA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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ENDOSCOPIC LIGHT SOURCE XL180/L3 (K023468)World of Medicine Lemke GmbH2003-01-14
ENDOSCOPIC LIGHT SOURCE, MODEL XL300/L5 (K021717)World of Medicine Lemke GmbH2002-08-20
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LUMENON XENON LIGHT SOURCE (K992050)Walter Lorenz Surgical, Inc.1999-09-14
XENON LIGHT SOURCE PES 1 (K992540)Laser Optik Systeme GmbH & Co. KG1999-09-14
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Recalls involving this device

No recalls on record reference this clearance.