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FDA 510(k)

IFA SENSIBAC CEPHALOTIN

K-Number: K892735 · 1989-08-17

ApplicantInvestigacion Farmaceutica S.A. DE C.V.
Decision Date1989-08-17
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IFA SENSIBAC CEPHALOTIN 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 1989-08-17 under 510(k) number K892735. 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 CEPHALOTIN?

IFA SENSIBAC CEPHALOTIN is a medical device that received FDA 510(k) clearance on 1989-08-17. The listed applicant is Investigacion Farmaceutica S.A. DE C.V.. The 510(k) number is K892735.

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

IFA SENSIBAC CEPHALOTIN received FDA 510(k) clearance on 1989-08-17, under 510(k) number K892735.

Who is the listed applicant for IFA SENSIBAC CEPHALOTIN?

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 CEPHALOTIN?

The FDA product code for IFA SENSIBAC CEPHALOTIN 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.

K892721IFA SENSIBAC CEFACLORK892728IFA SENSIBAC NORFLOXACINK892733IFA SENSIBAC KANAMYCINK892713IFA SENSIBAC NALIDIXIC ACIDK885110PROTEUS OX-19 IFA*K885113IFA* POSITIVE AND NEGATIVE ANTIGENS CONTROL

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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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