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FDA 510(k)

I.V. ADMINISTRATION SETS

K-Number: K955821 · 1996-07-10

Decision Date1996-07-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. ADMINISTRATION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Associates Network, Inc.. It received FDA 510(k) clearance on 1996-07-10 under 510(k) number K955821. 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 I.V. ADMINISTRATION SETS?

I.V. ADMINISTRATION SETS is a medical device that received FDA 510(k) clearance on 1996-07-10. The listed applicant is Medical Associates Network, Inc.. The 510(k) number is K955821.

When did I.V. ADMINISTRATION SETS receive FDA 510(k) clearance?

I.V. ADMINISTRATION SETS received FDA 510(k) clearance on 1996-07-10, under 510(k) number K955821.

Who is the listed applicant for I.V. ADMINISTRATION SETS?

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

What is the FDA product code for I.V. ADMINISTRATION SETS?

The FDA product code for I.V. ADMINISTRATION SETS 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 Associates Network, 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.

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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