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FDA 510(k)

MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER

K-Number: K910227 · 1991-04-03

ApplicantMedex, Inc.
Decision Date1991-04-03
Product CodeKXO
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1991-04-03 under 510(k) number K910227. 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 MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER?

MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER is a medical device that received FDA 510(k) clearance on 1991-04-03. The listed applicant is Medex, Inc.. The 510(k) number is K910227.

When did MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER receive FDA 510(k) clearance?

MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER received FDA 510(k) clearance on 1991-04-03, under 510(k) number K910227.

Who is the listed applicant for MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER?

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

What is the FDA product code for MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER?

The FDA product code for MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER is KXO.

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.

Other records listing Medex, 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.

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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.

Official Source

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

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