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FDA 510(k)

FLU VEN I.V. SET 0153-C PERMA-SET

K-Number: K843692 · 1984-10-31

ApplicantVenusa , Ltd.
Decision Date1984-10-31
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLU VEN I.V. SET 0153-C PERMA-SET is the device name listed in this FDA 510(k) record. The listed applicant is Venusa , Ltd.. It received FDA 510(k) clearance on 1984-10-31 under 510(k) number K843692. 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 FLU VEN I.V. SET 0153-C PERMA-SET?

FLU VEN I.V. SET 0153-C PERMA-SET is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is Venusa , Ltd.. The 510(k) number is K843692.

When did FLU VEN I.V. SET 0153-C PERMA-SET receive FDA 510(k) clearance?

FLU VEN I.V. SET 0153-C PERMA-SET received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843692.

Who is the listed applicant for FLU VEN I.V. SET 0153-C PERMA-SET?

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

What is the FDA product code for FLU VEN I.V. SET 0153-C PERMA-SET?

The FDA product code for FLU VEN I.V. SET 0153-C PERMA-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 Venusa , Ltd. 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 8 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

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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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