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FDA 510(k)

MMI/GAELTEC CATHETER INTRAUTERINE

K-Number: K801758 · 1980-08-14

ApplicantMedical Measurements, Inc.
Decision Date1980-08-14
Product CodeKXO
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MMI/GAELTEC CATHETER INTRAUTERINE 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 K801758. The device is classified under product code KXO. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMI/GAELTEC CATHETER INTRAUTERINE?

MMI/GAELTEC CATHETER INTRAUTERINE 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 K801758.

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

MMI/GAELTEC CATHETER INTRAUTERINE received FDA 510(k) clearance on 1980-08-14, under 510(k) number K801758.

Who is the listed applicant for MMI/GAELTEC CATHETER INTRAUTERINE?

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 INTRAUTERINE?

The FDA product code for MMI/GAELTEC CATHETER INTRAUTERINE is KXO.

Related Clinical Trials

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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 TRANSDUCK801880MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS

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Related Devices (Code: KXO)

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.

K991235SOFTRANS TEMP INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS TEMP IUPC)Ludlow Technical ProductsK982565EASY TRANS TIPCarl SchuhK974730SOFTRANS PLUS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS PLUS IUPC)Graphic Controls Corp.K964279SOFTRANS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 4000 SOFTRANS IUPC)Graphic Controls Corp.K961290IUP - TIP TRANS, IUP - PROXI TRANSScientific Device Manufacturer, LLCK950498LIFE TRACE TRANS TIP INTRAUTERINE PRESSURE CATHETERGraphic Controls 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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