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FDA 510(k)

TRIP CIC CATHETER

K-Number: K920849 · 1995-03-17

ApplicantTonometrics, Inc.
Decision Date1995-03-17
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRIP CIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Tonometrics, Inc.. It received FDA 510(k) clearance on 1995-03-17 under 510(k) number K920849. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIP CIC CATHETER?

TRIP CIC CATHETER is a medical device that received FDA 510(k) clearance on 1995-03-17. The listed applicant is Tonometrics, Inc.. The 510(k) number is K920849.

When did TRIP CIC CATHETER receive FDA 510(k) clearance?

TRIP CIC CATHETER received FDA 510(k) clearance on 1995-03-17, under 510(k) number K920849.

Who is the listed applicant for TRIP CIC CATHETER?

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

What is the FDA product code for TRIP CIC CATHETER?

The FDA product code for TRIP CIC CATHETER is FFT.

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 Tonometrics, 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.

K911825TRIP(TM) NASOGASTRIC SUMP CATHETERK890466SIGMOID TONOMITORK883234TONOMITOR (TM) + SUMP

Related Devices (Code: FFT)

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.

K102543BRAVO PH MONITORING SYSTEM AND ACCESSORIESGiven Imaging , Ltd.K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBESandhill Scientific, Inc.K002028BRAVO PH MONITORING SYSTEMEndonetics, Inc.K961346PH ANALYSIS MODULESynectics-DantecK950087LOT 440Medical Instruments Corporation Mic AGK955018TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATORInstrumentarium Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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