Atlas FDA

S1500 XENON LIGHT SOURCE

FDA 510(k) clearance K922837 · decided 1992-11-03

Clearance details

K-number
K922837
Device name
S1500 XENON LIGHT SOURCE
Applicant
Endomedix
Decision
Substantially Equivalent
Date received
1992-06-12
Decision date
1992-11-03
Days to decision
144 days
Clearance type
Traditional
Product code
HBI
Device class
2
Regulation number
878.4580
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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LIGHT GUIDE CABLE (K111342)Schott North America2011-11-25
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ENDOSCOPIC FIBEROPTIC CABLE (K021931)Gulf Medical Fiberoptics2002-09-06
ENDOSCOPIC FIBEROPTIC CABLE (K991208)Isolux America1999-06-23
LIGHTSOURCE OR ILLUMINATOR MODEL I-100 (K983277)Cuda Products Co.1998-12-16
LUMINOUS 150 FIBEROPTIC ILLUMINATOR (K933593)Progressive Dynamics, Inc.1993-10-28
NEXTEC FIBEROPTIC CABLES (K922462)Nextec Corp.1992-09-21
LUMINOUS 250 FIBEROPTIC ILLUMINATOR (K921866)Progressive Dynamics, Inc.1992-07-08
NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL (K920167)Nextec Corp.1992-03-23

Recalls involving this device

No recalls on record reference this clearance.