ALPHA MICRON-40 FILTER
K-Number: K810761 · 1981-06-30
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Device Summary
Frequently Asked Questions
What is the ALPHA MICRON-40 FILTER?
ALPHA MICRON-40 FILTER is a medical device that received FDA 510(k) clearance on 1981-06-30. The listed applicant is Alpha Therapeutic Corp.. The 510(k) number is K810761.
When did ALPHA MICRON-40 FILTER receive FDA 510(k) clearance?
ALPHA MICRON-40 FILTER received FDA 510(k) clearance on 1981-06-30, under 510(k) number K810761.
Who is the listed applicant for ALPHA MICRON-40 FILTER?
The FDA 510(k) record lists Alpha Therapeutic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALPHA MICRON-40 FILTER?
The FDA product code for ALPHA MICRON-40 FILTER is CAK.
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 Alpha Therapeutic Corp. 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: CAK)
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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