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FDA 510(k)

THROMBOSTIN IFA*

K-Number: K885107 · 1989-06-23

ApplicantInvestigacion Farmaceutica S.A. DE C.V.
Decision Date1989-06-23
Product CodeGJS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

THROMBOSTIN 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 1989-06-23 under 510(k) number K885107. The device is classified under product code GJS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROMBOSTIN IFA*?

THROMBOSTIN IFA* is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Investigacion Farmaceutica S.A. DE C.V.. The 510(k) number is K885107.

When did THROMBOSTIN IFA* receive FDA 510(k) clearance?

THROMBOSTIN IFA* received FDA 510(k) clearance on 1989-06-23, under 510(k) number K885107.

Who is the listed applicant for THROMBOSTIN 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 THROMBOSTIN IFA*?

The FDA product code for THROMBOSTIN IFA* is GJS.

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Other records listing Investigacion Farmaceutica S.A. DE C.V. as applicant

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Related Devices (Code: GJS)

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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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