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FDA 510(k)

BRUCELLA IFA*

K-Number: K885112 · 1989-08-15

Decision Date1989-08-15
Product CodeGSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BRUCELLA 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 K885112. The device is classified under product code GSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUCELLA IFA*?

BRUCELLA 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 K885112.

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

BRUCELLA IFA* received FDA 510(k) clearance on 1989-08-15, under 510(k) number K885112.

Who is the listed applicant for BRUCELLA 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 BRUCELLA IFA*?

The FDA product code for BRUCELLA IFA* is GSO.

Related Clinical Trials

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.

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

View all 24 devices →

Related Devices (Code: GSO)

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.

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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