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FDA 510(k)

OHMEDA MODEL 4700 OXICAP

K-Number: K911193 · 1991-08-02

ApplicantOhmeda Medical
Decision Date1991-08-02
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA MODEL 4700 OXICAP is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1991-08-02 under 510(k) number K911193. 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 4700 OXICAP?

OHMEDA MODEL 4700 OXICAP is a medical device that received FDA 510(k) clearance on 1991-08-02. The listed applicant is Ohmeda Medical. The 510(k) number is K911193.

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

OHMEDA MODEL 4700 OXICAP received FDA 510(k) clearance on 1991-08-02, under 510(k) number K911193.

Who is the listed applicant for OHMEDA MODEL 4700 OXICAP?

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 4700 OXICAP?

The FDA product code for OHMEDA MODEL 4700 OXICAP is CCK.

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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: 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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