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FDA 510(k)

PROTEUS OX-19 IFA*

K-Number: K885110 · 1989-08-15

ApplicantInvestigacion Farmaceutica S.A. DE C.V.
Decision Date1989-08-15
Product CodeGSZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PROTEUS OX-19 IFA* is the device name listed in this FDA 510(k) record. The listed applicant is Investigacion Farmaceutica S.A. DE C.V.. It received FDA 510(k) clearance on 1989-08-15 under 510(k) number K885110. The device is classified under product code GSZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTEUS OX-19 IFA*?

PROTEUS OX-19 IFA* is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Investigacion Farmaceutica S.A. DE C.V.. The 510(k) number is K885110.

When did PROTEUS OX-19 IFA* receive FDA 510(k) clearance?

PROTEUS OX-19 IFA* received FDA 510(k) clearance on 1989-08-15, under 510(k) number K885110.

Who is the listed applicant for PROTEUS OX-19 IFA*?

The FDA 510(k) record lists Investigacion Farmaceutica S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROTEUS OX-19 IFA*?

The FDA product code for PROTEUS OX-19 IFA* is GSZ.

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Related Devices (Code: GSZ)

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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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