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FDA 510(k)

OHMEDA MODEL 5250 RGM MONITOR

K-Number: K920590 · 1992-08-31

ApplicantOhmeda Medical
Decision Date1992-08-31
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA MODEL 5250 RGM MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1992-08-31 under 510(k) number K920590. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA MODEL 5250 RGM MONITOR?

OHMEDA MODEL 5250 RGM MONITOR is a medical device that received FDA 510(k) clearance on 1992-08-31. The listed applicant is Ohmeda Medical. The 510(k) number is K920590.

When did OHMEDA MODEL 5250 RGM MONITOR receive FDA 510(k) clearance?

OHMEDA MODEL 5250 RGM MONITOR received FDA 510(k) clearance on 1992-08-31, under 510(k) number K920590.

Who is the listed applicant for OHMEDA MODEL 5250 RGM MONITOR?

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 OHMEDA MODEL 5250 RGM MONITOR?

The FDA product code for OHMEDA MODEL 5250 RGM MONITOR is CCK.

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Other records listing Ohmeda Medical as applicant

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Related Devices (Code: CCK)

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.

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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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