Atlas FDA

NEXTEC FIBEROPTIC CABLES

FDA 510(k) clearance K922462 · decided 1992-09-21

Clearance details

K-number
K922462
Device name
NEXTEC FIBEROPTIC CABLES
Applicant
Nextec Corp.
Decision
Substantially Equivalent
Date received
1992-05-26
Decision date
1992-09-21
Days to decision
118 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
Naples, 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
Light-Guide Cables (K223183)Olympus Winter & Ibe GmbH2023-01-13
OptiLux LED Illuminator (K163185)Isolux, LLC2016-11-21
KOGENT SPETZLER LIGHTED SUCTION TUBES (K141781)Katalyst Surgical, LLC2015-04-09
LIGHT GUIDE CABLE (K111342)Schott North America2011-11-25
1125 XSB XENON FIBER-OPTIC LIGHT SOURCE (K052979)Isolux, LLC2005-10-31
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
S1500 XENON LIGHT SOURCE (K922837)Endomedix1992-11-03
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.