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FDA 510(k)

IFA SENSIBAC ERYTHROMYCIN

K-Number: K892719 · 1989-08-03

ApplicantInvestigacion Farmaceutica S.A. DE C.V.
Decision Date1989-08-03
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IFA SENSIBAC ERYTHROMYCIN 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 1989-08-03 under 510(k) number K892719. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IFA SENSIBAC ERYTHROMYCIN?

IFA SENSIBAC ERYTHROMYCIN is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Investigacion Farmaceutica S.A. DE C.V.. The 510(k) number is K892719.

When did IFA SENSIBAC ERYTHROMYCIN receive FDA 510(k) clearance?

IFA SENSIBAC ERYTHROMYCIN received FDA 510(k) clearance on 1989-08-03, under 510(k) number K892719.

Who is the listed applicant for IFA SENSIBAC ERYTHROMYCIN?

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 IFA SENSIBAC ERYTHROMYCIN?

The FDA product code for IFA SENSIBAC ERYTHROMYCIN is JTN.

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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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Related Devices (Code: JTN)

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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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