Atlas FDA

XENON LIGHT SOURCE MODEL LS6000

FDA 510(k) clearance K981804 · decided 1998-07-24

Clearance details

K-number
K981804
Device name
XENON LIGHT SOURCE MODEL LS6000
Applicant
Contec Medical Vision, Ltd.
Decision
Substantially Equivalent
Date received
1998-05-21
Decision date
1998-07-24
Days to decision
64 days
Clearance type
Traditional
Product code
GCT
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Fallston,, MD, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ALPHAXENON LIGHT 180 W AND 300 W (K093125)Gimmi GmbH2010-01-27
XENON-100 SCB LIGHT SOURCE, MODEL 20132620 (K082925)KARL STORZ Endoscopy-America, Inc.2008-12-18
CONMED LINVATEC 300W XENON LIGHT SOURCE (K070376)Conmed Linvatec2007-08-20
VIADUCT MINISCOPE AND ACCESSORIES (K040949)Acueity, Inc.2004-05-07
KSEA MEDI PACK (K022490)KARL STORZ Endoscopy-America, Inc.2003-09-29
LINVATEC 300W XENON LIGHT SOURCE (K031994)Linvatec Corp.2003-08-21
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
ENDOSCOPIC LIGHT SOURCE XL202/L3 (K020889)World of Medicine Lemke GmbH2002-06-05
DAYLITE XENON LIGHT SOURCES (K013880)Designs For Vision, Inc.2001-12-07
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

Recalls involving this device

No recalls on record reference this clearance.