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FDA 510(k)

SALMONELLA IFA*

K-Number: K885114 · 1989-08-15

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

Device Summary

SALMONELLA 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 K885114. The device is classified under product code GHC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALMONELLA IFA*?

SALMONELLA 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 K885114.

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

SALMONELLA IFA* received FDA 510(k) clearance on 1989-08-15, under 510(k) number K885114.

Who is the listed applicant for SALMONELLA 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 SALMONELLA IFA*?

The FDA product code for SALMONELLA IFA* is GHC.

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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.

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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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