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FDA 510(k)

PRN PLUS + INFUSION SET

K-Number: K884053 · 1988-10-31

Decision Date1988-10-31
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRN PLUS + INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Prn Services, Inc.. It received FDA 510(k) clearance on 1988-10-31 under 510(k) number K884053. 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 PRN PLUS + INFUSION SET?

PRN PLUS + INFUSION SET is a medical device that received FDA 510(k) clearance on 1988-10-31. The listed applicant is Prn Services, Inc.. The 510(k) number is K884053.

When did PRN PLUS + INFUSION SET receive FDA 510(k) clearance?

PRN PLUS + INFUSION SET received FDA 510(k) clearance on 1988-10-31, under 510(k) number K884053.

Who is the listed applicant for PRN PLUS + INFUSION SET?

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

What is the FDA product code for PRN PLUS + INFUSION SET?

The FDA product code for PRN PLUS + 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 Prn Services, 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 7 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

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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