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FDA 510(k)

BACTROL TB SLIDE

K-Number: K833900 · 1983-12-22

ApplicantDifco Laboratories, Inc.
Decision Date1983-12-22
Product Code
DecisionSubstantially Equivalent

Device Summary

BACTROL TB SLIDE 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 1983-12-22 under 510(k) number K833900. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTROL TB SLIDE?

BACTROL TB SLIDE is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K833900.

When did BACTROL TB SLIDE receive FDA 510(k) clearance?

BACTROL TB SLIDE received FDA 510(k) clearance on 1983-12-22, under 510(k) number K833900.

Who is the listed applicant for BACTROL TB SLIDE?

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

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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.

K971120DISPENS-O-DISC (TM) LEVOFLOXACINK971211DISPENS-O-DISC SPARFLOXACINK963508DISPENS-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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