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FDA 510(k)

MC/CPAP MANIFOLD

K-Number: K874479 · 1987-12-30

Decision Date1987-12-30
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MC/CPAP MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Minneapolis Children'S Services Corp.. It received FDA 510(k) clearance on 1987-12-30 under 510(k) number K874479. The device is classified under product code BYE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MC/CPAP MANIFOLD?

MC/CPAP MANIFOLD is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Minneapolis Children'S Services Corp.. The 510(k) number is K874479.

When did MC/CPAP MANIFOLD receive FDA 510(k) clearance?

MC/CPAP MANIFOLD received FDA 510(k) clearance on 1987-12-30, under 510(k) number K874479.

Who is the listed applicant for MC/CPAP MANIFOLD?

The FDA 510(k) record lists Minneapolis Children'S Services Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MC/CPAP MANIFOLD?

The FDA product code for MC/CPAP MANIFOLD is BYE.

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.

Related Devices (Code: BYE)

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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