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FDA 510(k)

IV SET

K-Number: K901949 · 1990-09-12

ApplicantJfv, Inc.
Decision Date1990-09-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV SET is the device name listed in this FDA 510(k) record. The listed applicant is Jfv, Inc.. It received FDA 510(k) clearance on 1990-09-12 under 510(k) number K901949. 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 IV SET?

IV SET is a medical device that received FDA 510(k) clearance on 1990-09-12. The listed applicant is Jfv, Inc.. The 510(k) number is K901949.

When did IV SET receive FDA 510(k) clearance?

IV SET received FDA 510(k) clearance on 1990-09-12, under 510(k) number K901949.

Who is the listed applicant for IV SET?

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

What is the FDA product code for IV SET?

The FDA product code for IV SET is FPA.

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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