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FDA 510(k)

BORNING NEONATAL RESUSCITATOIN CENTER

K-Number: K850069 · 1985-05-30

ApplicantBorning Corp.
Decision Date1985-05-30
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BORNING NEONATAL RESUSCITATOIN CENTER is the device name listed in this FDA 510(k) record. The listed applicant is Borning Corp.. It received FDA 510(k) clearance on 1985-05-30 under 510(k) number K850069. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BORNING NEONATAL RESUSCITATOIN CENTER?

BORNING NEONATAL RESUSCITATOIN CENTER is a medical device that received FDA 510(k) clearance on 1985-05-30. The listed applicant is Borning Corp.. The 510(k) number is K850069.

When did BORNING NEONATAL RESUSCITATOIN CENTER receive FDA 510(k) clearance?

BORNING NEONATAL RESUSCITATOIN CENTER received FDA 510(k) clearance on 1985-05-30, under 510(k) number K850069.

Who is the listed applicant for BORNING NEONATAL RESUSCITATOIN CENTER?

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

What is the FDA product code for BORNING NEONATAL RESUSCITATOIN CENTER?

The FDA product code for BORNING NEONATAL RESUSCITATOIN CENTER is FMT.

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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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