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FDA 510(k)

VENUSA, LTD. EXTENSION SET WITH FILTER

K-Number: K994429 · 2000-03-03

ApplicantVenusa , Ltd.
Decision Date2000-03-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENUSA, LTD. EXTENSION SET WITH FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Venusa , Ltd.. It received FDA 510(k) clearance on 2000-03-03 under 510(k) number K994429. 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 VENUSA, LTD. EXTENSION SET WITH FILTER?

VENUSA, LTD. EXTENSION SET WITH FILTER is a medical device that received FDA 510(k) clearance on 2000-03-03. The listed applicant is Venusa , Ltd.. The 510(k) number is K994429.

When did VENUSA, LTD. EXTENSION SET WITH FILTER receive FDA 510(k) clearance?

VENUSA, LTD. EXTENSION SET WITH FILTER received FDA 510(k) clearance on 2000-03-03, under 510(k) number K994429.

Who is the listed applicant for VENUSA, LTD. EXTENSION SET WITH FILTER?

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 VENUSA, LTD. EXTENSION SET WITH FILTER?

The FDA product code for VENUSA, LTD. EXTENSION SET WITH FILTER 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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