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FDA 510(k)

OHIO CARE PLUS INCUBATOR

K-Number: K943360 · 1994-09-29

Decision Date1994-09-29
Product CodeFMZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OHIO CARE PLUS INCUBATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K943360. The device is classified under product code FMZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO CARE PLUS INCUBATOR?

OHIO CARE PLUS INCUBATOR is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Ohmeda Medical. The 510(k) number is K943360.

When did OHIO CARE PLUS INCUBATOR receive FDA 510(k) clearance?

OHIO CARE PLUS INCUBATOR received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943360.

Who is the listed applicant for OHIO CARE PLUS INCUBATOR?

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

What is the FDA product code for OHIO CARE PLUS INCUBATOR?

The FDA product code for OHIO CARE PLUS INCUBATOR is FMZ.

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.

Other records listing Ohmeda Medical as applicant

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.

View all 119 devices →

Related Devices (Code: FMZ)

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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