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FDA 510(k)

CEFUROXIME 30MCG. SENSITIVITY DISCS

K-Number: K832909 · 1983-10-14

Decision Date1983-10-14
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFUROXIME 30MCG. SENSITIVITY DISCS is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832909. 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 CEFUROXIME 30MCG. SENSITIVITY DISCS?

CEFUROXIME 30MCG. SENSITIVITY DISCS is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K832909.

When did CEFUROXIME 30MCG. SENSITIVITY DISCS receive FDA 510(k) clearance?

CEFUROXIME 30MCG. SENSITIVITY DISCS received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832909.

Who is the listed applicant for CEFUROXIME 30MCG. SENSITIVITY DISCS?

The FDA 510(k) record lists Difco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEFUROXIME 30MCG. SENSITIVITY DISCS?

The FDA product code for CEFUROXIME 30MCG. SENSITIVITY DISCS is JTN.

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 Difco Laboratories, Inc. 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 121 devices →

Related Devices (Code: JTN)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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