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FDA 510(k)

SUCTION GUILLOTINE DEVICE

K-Number: K932142 · 1993-09-24

ApplicantTriton Technology, Inc.
Decision Date1993-09-24
Product CodeFCK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUCTION GUILLOTINE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Triton Technology, Inc.. It received FDA 510(k) clearance on 1993-09-24 under 510(k) number K932142. The device is classified under product code FCK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION GUILLOTINE DEVICE?

SUCTION GUILLOTINE DEVICE is a medical device that received FDA 510(k) clearance on 1993-09-24. The listed applicant is Triton Technology, Inc.. The 510(k) number is K932142.

When did SUCTION GUILLOTINE DEVICE receive FDA 510(k) clearance?

SUCTION GUILLOTINE DEVICE received FDA 510(k) clearance on 1993-09-24, under 510(k) number K932142.

Who is the listed applicant for SUCTION GUILLOTINE DEVICE?

The FDA 510(k) record lists Triton Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION GUILLOTINE DEVICE?

The FDA product code for SUCTION GUILLOTINE DEVICE is FCK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Triton Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K911448MULTIPLE BIOPSY DEVICE-MBXK902883TISSUE/POLYP TRAP SYSTEMK881303TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER

Related Devices (Code: FCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K153763Howell Biliary Aspiration NeedleWilson-Cook Medical, Inc.K103326MULTIPLE BIOPSY SYSTEMUnited States Endoscopy Group, Inc.K062159RB12 SUCTION RECTAL BIOPSY SYSTEMAus Systems Pty , Ltd.K061201DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087United States Endoscopy Group, Inc.K051637DSNARE, MODEL 00711087United States Endoscopy Group, Inc.K954693MEHTA BRONCHIAL BIOSPY DRILLUnited States Endoscopy Group, Inc.

Official Source

View on FDA Database →

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