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FDA 510(k)

250 ML BAG W/Y INJECT. & 12 EXTENSION SET

K-Number: K882598 · 1988-11-01

Decision Date1988-11-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

250 ML BAG W/Y INJECT. & 12 EXTENSION 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 1988-11-01 under 510(k) number K882598. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 250 ML BAG W/Y INJECT. & 12 EXTENSION SET?

250 ML BAG W/Y INJECT. & 12 EXTENSION SET is a medical device that received FDA 510(k) clearance on 1988-11-01. The listed applicant is Prn Services, Inc.. The 510(k) number is K882598.

When did 250 ML BAG W/Y INJECT. & 12 EXTENSION SET receive FDA 510(k) clearance?

250 ML BAG W/Y INJECT. & 12 EXTENSION SET received FDA 510(k) clearance on 1988-11-01, under 510(k) number K882598.

Who is the listed applicant for 250 ML BAG W/Y INJECT. & 12 EXTENSION 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 250 ML BAG W/Y INJECT. & 12 EXTENSION SET?

The FDA product code for 250 ML BAG W/Y INJECT. & 12 EXTENSION SET is FRN.

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: FRN)

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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