MULTI HI-FLO PNEU, WISAP #7080
K-Number: K011510 · 2002-04-02
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Device Summary
Frequently Asked Questions
What is the MULTI HI-FLO PNEU, WISAP #7080?
MULTI HI-FLO PNEU, WISAP #7080 is a medical device that received FDA 510(k) clearance on 2002-04-02. The listed applicant is Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh. The 510(k) number is K011510.
When did MULTI HI-FLO PNEU, WISAP #7080 receive FDA 510(k) clearance?
MULTI HI-FLO PNEU, WISAP #7080 received FDA 510(k) clearance on 2002-04-02, under 510(k) number K011510.
Who is the listed applicant for MULTI HI-FLO PNEU, WISAP #7080?
The FDA 510(k) record lists Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI HI-FLO PNEU, WISAP #7080?
The FDA product code for MULTI HI-FLO PNEU, WISAP #7080 is HIF.
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 Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh 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: HIF)
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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