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FDA 510(k)

ANTI-FOR SURGICAL FACE MASK

K-Number: K905865 · 1991-03-06

ApplicantAnago, Inc.
Decision Date1991-03-06
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANTI-FOR SURGICAL FACE MASK is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1991-03-06 under 510(k) number K905865. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-FOR SURGICAL FACE MASK?

ANTI-FOR SURGICAL FACE MASK is a medical device that received FDA 510(k) clearance on 1991-03-06. The listed applicant is Anago, Inc.. The 510(k) number is K905865.

When did ANTI-FOR SURGICAL FACE MASK receive FDA 510(k) clearance?

ANTI-FOR SURGICAL FACE MASK received FDA 510(k) clearance on 1991-03-06, under 510(k) number K905865.

Who is the listed applicant for ANTI-FOR SURGICAL FACE MASK?

The FDA 510(k) record lists Anago, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTI-FOR SURGICAL FACE MASK?

The FDA product code for ANTI-FOR SURGICAL FACE MASK is FXX.

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 Anago, Inc. 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.

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Related Devices (Code: FXX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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