Atlas FDA

GABRIEL URETERAL ILLUMINATOR SYSTEM

FDA 510(k) clearance K940019 · decided 1994-05-02

Clearance details

K-number
K940019
Device name
GABRIEL URETERAL ILLUMINATOR SYSTEM
Applicant
Gabriel Medical, Inc.
Decision
Substantially Equivalent
Date received
1994-01-03
Decision date
1994-05-02
Days to decision
119 days
Clearance type
Traditional
Product code
FCS
Device class
2
Regulation number
876.4020
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
North Attleboro, MA, 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
STRYKER INFRARED ILLUMINATION SYSTEM (IRIS) [AIM Light Source and IRIS Ureteral Kit] (K151243)Stryker Endoscopy2015-08-20
STRYKER URETERAL ILLUMINATION SYSTEM IV (K061548)Stryker Corp.2006-09-28
STRYKER URETERAL ILLUMINATOR SYSTEM III (K982542)Stryker Endoscopy1998-09-22
URIGLOW TRANSILLUMINATING URETERIC STENT MODEL (K943801)Rocket of London, Ltd.1995-08-15
GABRIEL URETERAL ILLUMINATOR SYSTEM II (K945088)Gabriel Medical, Inc.1995-02-07
URETERAL ILLUMINATOR (K941506)Apple Medical Corp.1994-10-05
ILLUMINATED URETERAL CATHETER (K923436)Cook Urological, Inc.1993-03-05
LASEGUIDE 600A, 600B, 400A, AND 400B (K874680)Laser Peripherals, LLC1988-03-23
SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE (K880071)Laserguide1988-03-22

Recalls involving this device

No recalls on record reference this clearance.