Atlas FDA

LED LIGHT SOURCE

FDA 510(k) clearance K093792 · decided 2010-03-18

Clearance details

K-number
K093792
Device name
LED LIGHT SOURCE
Applicant
Sunoptic Technologies, LLC
Decision
Substantially Equivalent
Date received
2009-12-10
Decision date
2010-03-18
Days to decision
98 days
Clearance type
Traditional
Product code
FCW
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Jacksonville, FL, 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
NOVAPROBE LED LIGHT SOURCE (K131226)Novaprobe Incorporated2014-07-24
POWER LED 175 (K123956)KARL STORZ Endoscopy-America, Inc.2013-01-25
OVS1 VIDEO SYSTEM (K123359)Olive Medical Corp.2012-12-19
ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 (K121724)Richard Wolf Medical Instruments Corp.2012-09-20
KARL STORZ LED NOVA 100 COLD LIGHT FOUNTAIN, MODELS 2016020, 20161020C (K091968)KARL STORZ Endoscopy-America, Inc.2009-09-14
STRYKER LED LIGHTSOURCE (K082813)Stryker Corp.2008-12-19
LUXTEC MLX LIGHT SOURCE (K081477)Integra Luxtec, Inc.2008-06-18
ACUEITY MEDICAL LIGHT SOURCE (K032430)Acueity, Inc.2003-09-05
METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 (K012265)Circon Video2001-10-17
VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE (K000229)Videolabs, Inc.2000-03-21
COLDLIGHTSOURCE PL3000 (K993300)Fiber Imaging Technologies, Inc.1999-11-05
50 W METAL HALIDE ILLUMINATOR, VES 0501. (K992447)Angiolaz, Inc.1999-10-20

Recalls involving this device

No recalls on record reference this clearance.