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FDA 510(k)

OXLIFE

K-Number: K904271 · 1990-10-12

ApplicantMedical Repair Service, Inc.
Decision Date1990-10-12
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXLIFE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Repair Service, Inc.. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K904271. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXLIFE?

OXLIFE is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Medical Repair Service, Inc.. The 510(k) number is K904271.

When did OXLIFE receive FDA 510(k) clearance?

OXLIFE received FDA 510(k) clearance on 1990-10-12, under 510(k) number K904271.

Who is the listed applicant for OXLIFE?

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

What is the FDA product code for OXLIFE?

The FDA product code for OXLIFE is CAW.

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Related Devices (Code: CAW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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