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FDA 510(k)

FLU VEN 0160

K-Number: K770863 · 1977-06-14

Decision Date1977-06-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLU VEN 0160 is the device name listed in this FDA 510(k) record. The listed applicant is Venospital, Inc.. It received FDA 510(k) clearance on 1977-06-14 under 510(k) number K770863. 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 0160?

FLU VEN 0160 is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is Venospital, Inc.. The 510(k) number is K770863.

When did FLU VEN 0160 receive FDA 510(k) clearance?

FLU VEN 0160 received FDA 510(k) clearance on 1977-06-14, under 510(k) number K770863.

Who is the listed applicant for FLU VEN 0160?

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

What is the FDA product code for FLU VEN 0160?

The FDA product code for FLU VEN 0160 is FPA.

Other records listing Venospital, 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 14 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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