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FDA 510(k)

MX710 SERIES VASCULAR ACCESS INFUSION SET

K-Number: K874133 · 1988-01-14

ApplicantMedex, Inc.
Decision Date1988-01-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MX710 SERIES VASCULAR ACCESS INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1988-01-14 under 510(k) number K874133. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MX710 SERIES VASCULAR ACCESS INFUSION SET?

MX710 SERIES VASCULAR ACCESS INFUSION SET is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Medex, Inc.. The 510(k) number is K874133.

When did MX710 SERIES VASCULAR ACCESS INFUSION SET receive FDA 510(k) clearance?

MX710 SERIES VASCULAR ACCESS INFUSION SET received FDA 510(k) clearance on 1988-01-14, under 510(k) number K874133.

Who is the listed applicant for MX710 SERIES VASCULAR ACCESS INFUSION SET?

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 MX710 SERIES VASCULAR ACCESS INFUSION SET?

The FDA product code for MX710 SERIES VASCULAR ACCESS INFUSION SET is FPA.

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.

View all 48 devices →

Related Devices (Code: FPA)

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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