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FDA 510(k)

FACE MASK

K-Number: K890016 · 1989-02-03

ApplicantAnjudd Intl.
Decision Date1989-02-03
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FACE MASK is the device name listed in this FDA 510(k) record. The listed applicant is Anjudd Intl.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K890016. 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 FACE MASK?

FACE MASK is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Anjudd Intl.. The 510(k) number is K890016.

When did FACE MASK receive FDA 510(k) clearance?

FACE MASK received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890016.

Who is the listed applicant for FACE MASK?

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

What is the FDA product code for FACE MASK?

The FDA product code for FACE MASK is FXX.

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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