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FDA 510(k)

TB SUSCEPTIBILITY QUADS I AND II

K-Number: K920143 · 1992-06-09

ApplicantRemel Co.
Decision Date1992-06-09
Product CodeMJD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TB SUSCEPTIBILITY QUADS I AND II is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1992-06-09 under 510(k) number K920143. The device is classified under product code MJD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TB SUSCEPTIBILITY QUADS I AND II?

TB SUSCEPTIBILITY QUADS I AND II is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is Remel Co.. The 510(k) number is K920143.

When did TB SUSCEPTIBILITY QUADS I AND II receive FDA 510(k) clearance?

TB SUSCEPTIBILITY QUADS I AND II received FDA 510(k) clearance on 1992-06-09, under 510(k) number K920143.

Who is the listed applicant for TB SUSCEPTIBILITY QUADS I AND II?

The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TB SUSCEPTIBILITY QUADS I AND II?

The FDA product code for TB SUSCEPTIBILITY QUADS I AND II is MJD.

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Other records listing Remel Co. 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.

K013711BACTI-SWAB DRYK965151A.C.T. IIIK965150A.C.T. IVK965152A.C.T. IIK965149A.C.T. IK960090CALCOFLUOR WHITE STAIN KIT

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Related Devices (Code: MJD)

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.

K840981NIACIN REAGENT STRIPRemel Co.K823859MIDDLEBROOK 7H10 AGAR BASE-LOWPHGibco Laboratories Life Technologies, Inc.

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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