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FDA 510(k)

MMI/GAELTEC CATHETER TIP TRANSDUC

K-Number: K801756 · 1980-08-20

ApplicantMedical Measurements, Inc.
Decision Date1980-08-20
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MMI/GAELTEC CATHETER TIP TRANSDUC 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 1980-08-20 under 510(k) number K801756. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMI/GAELTEC CATHETER TIP TRANSDUC?

MMI/GAELTEC CATHETER TIP TRANSDUC is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Medical Measurements, Inc.. The 510(k) number is K801756.

When did MMI/GAELTEC CATHETER TIP TRANSDUC receive FDA 510(k) clearance?

MMI/GAELTEC CATHETER TIP TRANSDUC received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801756.

Who is the listed applicant for MMI/GAELTEC CATHETER TIP TRANSDUC?

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 TRANSDUC?

The FDA product code for MMI/GAELTEC CATHETER TIP TRANSDUC is DXO.

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.

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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. EPIDURALK801757MMI/GAELTEC CATHETER TIP PRESS. TRANSDUK801758MMI/GAELTEC CATHETER INTRAUTERINEK801880MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS

View all 8 devices →

Related Devices (Code: DXO)

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.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, Inc.

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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