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FDA 510(k)

OHMEDA 4700 OXICAP MONITOR

K-Number: K873199 · 1988-02-02

ApplicantOhmeda Medical
Decision Date1988-02-02
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OHMEDA 4700 OXICAP 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 1988-02-02 under 510(k) number K873199. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA 4700 OXICAP MONITOR?

OHMEDA 4700 OXICAP MONITOR is a medical device that received FDA 510(k) clearance on 1988-02-02. The listed applicant is Ohmeda Medical. The 510(k) number is K873199.

When did OHMEDA 4700 OXICAP MONITOR receive FDA 510(k) clearance?

OHMEDA 4700 OXICAP MONITOR received FDA 510(k) clearance on 1988-02-02, under 510(k) number K873199.

Who is the listed applicant for OHMEDA 4700 OXICAP 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 4700 OXICAP MONITOR?

The FDA product code for OHMEDA 4700 OXICAP MONITOR is DQA.

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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.

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Related Devices (Code: DQA)

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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