AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM
K-Number: K912651 · 1991-07-08
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Device Summary
Frequently Asked Questions
What is the AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM?
AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM is a medical device that received FDA 510(k) clearance on 1991-07-08. The listed applicant is Stackhouse Assoc.. The 510(k) number is K912651.
When did AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM receive FDA 510(k) clearance?
AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM received FDA 510(k) clearance on 1991-07-08, under 510(k) number K912651.
Who is the listed applicant for AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM?
The FDA 510(k) record lists Stackhouse Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM?
The FDA product code for AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM is FYD.
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 Stackhouse Assoc. 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: FYD)
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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