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FDA 510(k)

E-Z FLO + SET

K-Number: K902330 · 1990-09-21

Decision Date1990-09-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

E-Z FLO + 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 1990-09-21 under 510(k) number K902330. 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 E-Z FLO + SET?

E-Z FLO + SET is a medical device that received FDA 510(k) clearance on 1990-09-21. The listed applicant is Prn Services, Inc.. The 510(k) number is K902330.

When did E-Z FLO + SET receive FDA 510(k) clearance?

E-Z FLO + SET received FDA 510(k) clearance on 1990-09-21, under 510(k) number K902330.

Who is the listed applicant for E-Z FLO + 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 E-Z FLO + SET?

The FDA product code for E-Z FLO + SET is FPA.

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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