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FDA 510(k)

ALPHA MICRON-40 FILTER

K-Number: K810761 · 1981-06-30

Decision Date1981-06-30
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALPHA MICRON-40 FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Alpha Therapeutic Corp.. It received FDA 510(k) clearance on 1981-06-30 under 510(k) number K810761. The device is classified under product code CAK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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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