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FDA 510(k)

MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS

K-Number: K801880 · 1980-08-14

ApplicantMedical Measurements, Inc.
Decision Date1980-08-14
Product CodeBYR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS 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 1980-08-14 under 510(k) number K801880. The device is classified under product code BYR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS?

MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS is a medical device that received FDA 510(k) clearance on 1980-08-14. The listed applicant is Medical Measurements, Inc.. The 510(k) number is K801880.

When did MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS receive FDA 510(k) clearance?

MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS received FDA 510(k) clearance on 1980-08-14, under 510(k) number K801880.

Who is the listed applicant for MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS?

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 SERIES 8T DIFF. PRESS. TRANS?

The FDA product code for MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS is BYR.

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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. TRANSDUK801756MMI/GAELTEC CATHETER TIP TRANSDUCK801758MMI/GAELTEC CATHETER INTRAUTERINE

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Related Devices (Code: BYR)

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.

K896718BICORE VARIFLEX(R) FLOW TRANSDUCERBicore Monitoring SystemsK790334DRAGER ORMDraeger Medical, 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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