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FDA 510(k)

OHMEDA CPU MONITOR

K-Number: K852504 · 1985-07-01

ApplicantOhmeda Medical
Decision Date1985-07-01
Product Code
DecisionSubstantially Equivalent

Device Summary

OHMEDA CPU 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 1985-07-01 under 510(k) number K852504. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA CPU MONITOR?

OHMEDA CPU MONITOR is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Ohmeda Medical. The 510(k) number is K852504.

When did OHMEDA CPU MONITOR receive FDA 510(k) clearance?

OHMEDA CPU MONITOR received FDA 510(k) clearance on 1985-07-01, under 510(k) number K852504.

Who is the listed applicant for OHMEDA CPU MONITOR?

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

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.

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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.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

View all 119 devices →

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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