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FDA 510(k)

INTRAVENOUS EXTENSION SET

K-Number: K895367 · 1989-10-06

Decision Date1989-10-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Product Specialists. It received FDA 510(k) clearance on 1989-10-06 under 510(k) number K895367. 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 INTRAVENOUS EXTENSION SET?

INTRAVENOUS EXTENSION SET is a medical device that received FDA 510(k) clearance on 1989-10-06. The listed applicant is Medical Product Specialists. The 510(k) number is K895367.

When did INTRAVENOUS EXTENSION SET receive FDA 510(k) clearance?

INTRAVENOUS EXTENSION SET received FDA 510(k) clearance on 1989-10-06, under 510(k) number K895367.

Who is the listed applicant for INTRAVENOUS EXTENSION SET?

The FDA 510(k) record lists Medical Product Specialists as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRAVENOUS EXTENSION SET?

The FDA product code for INTRAVENOUS EXTENSION 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 Medical Product Specialists 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.

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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