MC/CPAP MANIFOLD
K-Number: K874479 · 1987-12-30
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Device Summary
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
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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