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FDA 510(k)

THE BLUE MASK

K-Number: K782163 · 1979-03-01

Decision Date1979-03-01
Product CodeBSJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE BLUE MASK is the device name listed in this FDA 510(k) record. The listed applicant is Collectovac, Inc.. It received FDA 510(k) clearance on 1979-03-01 under 510(k) number K782163. The device is classified under product code BSJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE BLUE MASK?

THE BLUE MASK is a medical device that received FDA 510(k) clearance on 1979-03-01. The listed applicant is Collectovac, Inc.. The 510(k) number is K782163.

When did THE BLUE MASK receive FDA 510(k) clearance?

THE BLUE MASK received FDA 510(k) clearance on 1979-03-01, under 510(k) number K782163.

Who is the listed applicant for THE BLUE MASK?

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

What is the FDA product code for THE BLUE MASK?

The FDA product code for THE BLUE MASK is BSJ.

Related Devices (Code: BSJ)

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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