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FDA 510(k)

CEFTAZIDIME 30 MCG SENSITVITY DISCS

K-Number: K852835 · 1985-08-12

ApplicantDifco Laboratories, Inc.
Decision Date1985-08-12
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFTAZIDIME 30 MCG SENSITVITY 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 1985-08-12 under 510(k) number K852835. 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 CEFTAZIDIME 30 MCG SENSITVITY DISCS?

CEFTAZIDIME 30 MCG SENSITVITY DISCS is a medical device that received FDA 510(k) clearance on 1985-08-12. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K852835.

When did CEFTAZIDIME 30 MCG SENSITVITY DISCS receive FDA 510(k) clearance?

CEFTAZIDIME 30 MCG SENSITVITY DISCS received FDA 510(k) clearance on 1985-08-12, under 510(k) number K852835.

Who is the listed applicant for CEFTAZIDIME 30 MCG SENSITVITY 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 CEFTAZIDIME 30 MCG SENSITVITY DISCS?

The FDA product code for CEFTAZIDIME 30 MCG SENSITVITY DISCS is JTN.

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Other records listing Difco Laboratories, Inc. as applicant

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K971211DISPENS-O-DISC SPARFLOXACINK971120DISPENS-O-DISC (TM) LEVOFLOXACINK963508DISPENS-O-DISC MEROPENEMK961148CEFEPIME DISPANS-O-DISC (CEFEPLIME - 30MCG)K954783DRYSLIDE CARTARRHALISK954784DRYSIDE NEISSERIA

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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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