Atlas FDA

SATURN LIGHT

FDA 510(k) clearance K935102 · decided 1994-06-27

Clearance details

K-number
K935102
Device name
SATURN LIGHT
Applicant
Burton Medical Products Corp.
Decision
Substantially Equivalent
Date received
1993-10-22
Decision date
1994-06-27
Days to decision
248 days
Clearance type
Traditional
Product code
FTA
Device class
2
Regulation number
878.4580
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Van Nuys, CA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
Universal Light Handle Cover, Light Handle Cover (K150532)Key Surgical, Inc.2015-09-22
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IDSS SLC (K133413)Black Diamond Video2014-01-07
OASYS SURGICAL LIGHT CONTROLLER (K112133)Oasys Healthcare2012-03-01
EASYSUITE SURGICAL LIGHT CONTROL (ESLC) (K102791)Image Stream Medical, Inc.2010-11-23
MAINSTREAM OR SURGICAL LIGHT CONTROL (MSLC) (K081698)Image Stream Medical, Inc.2008-07-30
LIGHT GUARD LIGHT HANDLE AND LIGHT HANDLE COVER (K053321)Xodus Medical, Inc.2006-01-19
SCB/STERIS OR-LIGHT INTERFACE BOX (K051505)KARL STORZ Endoscopy-America, Inc.2005-08-11
KSEA SCB ACC CONTROL (K023704)KARL STORZ Endoscopy-America, Inc.2003-01-30
KSEA SCB MEDIA CONTROL (K020640)KARL STORZ Endoscopy-America, Inc.2002-05-28
DISPOSABLE LIGHT HANDLE AND ADAPTOR (K020304)Aspen Surgical Products, Inc.2002-02-14

Recalls involving this device

No recalls on record reference this clearance.