VENUSA, LTD. EXTENSION SET WITH FILTER
K-Number: K994429 · 2000-03-03
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Device Summary
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.
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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