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FDA 510(k)

PORT INFUSION SET (PIS) INFUSION SET (IS)

K-Number: K897065 · 1990-02-16

Decision Date1990-02-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PORT INFUSION SET (PIS) INFUSION SET (IS) 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 1990-02-16 under 510(k) number K897065. 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 PORT INFUSION SET (PIS) INFUSION SET (IS)?

PORT INFUSION SET (PIS) INFUSION SET (IS) is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Prn Services, Inc.. The 510(k) number is K897065.

When did PORT INFUSION SET (PIS) INFUSION SET (IS) receive FDA 510(k) clearance?

PORT INFUSION SET (PIS) INFUSION SET (IS) received FDA 510(k) clearance on 1990-02-16, under 510(k) number K897065.

Who is the listed applicant for PORT INFUSION SET (PIS) INFUSION SET (IS)?

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 PORT INFUSION SET (PIS) INFUSION SET (IS)?

The FDA product code for PORT INFUSION SET (PIS) INFUSION SET (IS) 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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