Atlas FDA

SUCTION GUILLOTINE DEVICE

FDA 510(k) clearance K932142 · decided 1993-09-24

Clearance details

K-number
K932142
Device name
SUCTION GUILLOTINE DEVICE
Applicant
Triton Technology, Inc.
Decision
Substantially Equivalent
Date received
1993-05-03
Decision date
1993-09-24
Days to decision
144 days
Clearance type
Traditional
Product code
FCK
Device class
2
Regulation number
876.1075
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Salem, OH, 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
Howell Biliary Aspiration Needle (K153763)Wilson-Cook Medical, Inc.2017-04-06
MULTIPLE BIOPSY SYSTEM (K103326)United States Endoscopy Group, Inc.2011-04-06
RB12 SUCTION RECTAL BIOPSY SYSTEM (K062159)Aus Systems Pty , Ltd.2006-09-05
DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087 (K061201)United States Endoscopy Group, Inc.2006-05-30
DSNARE, MODEL 00711087 (K051637)United States Endoscopy Group, Inc.2005-10-31
MEHTA BRONCHIAL BIOSPY DRILL (K954693)United States Endoscopy Group, Inc.1995-10-23
BIOPSY DEVICE ACCESSORY (K944252)Biopsys Medical, Inc.1994-12-05
MULTIPLE BIOPSY DEVICE-MBX (K911448)Triton Technology, Inc.1991-04-16
CYTOASPIRATOR (K902910)H & B Medical Technology, Inc.1991-01-16
MODEL TR RECTAL SUCTION BIOPSY TUBE (K902097)Medical Measurements, Inc.1990-07-27
SUCTION BIOPSY INSTRUMENT (K895420)Mill-Rose Laboratory1990-02-09
WILSON-COOK BILIARY AND GASTRIC ASPIRATION NEEDLE (K895900)Wilson-Cook Medical, Inc.1990-01-11

Recalls involving this device

No recalls on record reference this clearance.