Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MMI/GAELTEC CATHETER TIP PRESS. TRANSDU

K-Number: K801757 · 1980-08-27

ApplicantMedical Measurements, Inc.
Decision Date1980-08-27
Product CodeFES
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MMI/GAELTEC CATHETER TIP PRESS. TRANSDU is the device name listed in this FDA 510(k) record. The listed applicant is Medical Measurements, Inc.. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801757. The device is classified under product code FES. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMI/GAELTEC CATHETER TIP PRESS. TRANSDU?

MMI/GAELTEC CATHETER TIP PRESS. TRANSDU is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Medical Measurements, Inc.. The 510(k) number is K801757.

When did MMI/GAELTEC CATHETER TIP PRESS. TRANSDU receive FDA 510(k) clearance?

MMI/GAELTEC CATHETER TIP PRESS. TRANSDU received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801757.

Who is the listed applicant for MMI/GAELTEC CATHETER TIP PRESS. TRANSDU?

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

What is the FDA product code for MMI/GAELTEC CATHETER TIP PRESS. TRANSDU?

The FDA product code for MMI/GAELTEC CATHETER TIP PRESS. TRANSDU is FES.

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 Medical Measurements, 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.

K921062GAELTEC MPR SERIESK902097MODEL TR RECTAL SUCTION BIOPSY TUBEK863479MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURALK801756MMI/GAELTEC CATHETER TIP TRANSDUCK801758MMI/GAELTEC CATHETER INTRAUTERINEK801880MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS

View all 8 devices →

Related Devices (Code: FES)

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.

K890284URODEC 500Ferguson Medical

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.

↑