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FDA 510(k)

ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN

K-Number: K911392 · 1991-05-08

ApplicantAlamar
Decision Date1991-05-08
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN is the device name listed in this FDA 510(k) record. The listed applicant is Alamar. It received FDA 510(k) clearance on 1991-05-08 under 510(k) number K911392. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN?

ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN is a medical device that received FDA 510(k) clearance on 1991-05-08. The listed applicant is Alamar. The 510(k) number is K911392.

When did ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN receive FDA 510(k) clearance?

ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN received FDA 510(k) clearance on 1991-05-08, under 510(k) number K911392.

Who is the listed applicant for ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN?

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

What is the FDA product code for ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN?

The FDA product code for ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN is JWY.

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Other records listing Alamar 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.

K911390ANTIMICROBIAL SUSCEPT. TEST PANEL(TRIMETHOPRIM)K911391ANTIMICROBIAL SUSCEPT. TEST PANEL (CEFTIZOXIME)K911389ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (IMIPENEM)K910484ANTIMICROBIAL SUSCEPTIBILITY TEST PANELK910345ANTIMICROBIAL CEFOPERAZONEK910346ANTIMICROBIAL CEFTRIAXONE

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Related Devices (Code: JWY)

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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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