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FDA 510(k)

ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID

K-Number: K911559 · 1991-04-22

ApplicantAlamar Biosciences Laboratory, Inc.
Decision Date1991-04-22
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID is the device name listed in this FDA 510(k) record. The listed applicant is Alamar Biosciences Laboratory, Inc.. It received FDA 510(k) clearance on 1991-04-22 under 510(k) number K911559. 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 SUSCEPT. TEST PANEL CEFONICID?

ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID is a medical device that received FDA 510(k) clearance on 1991-04-22. The listed applicant is Alamar Biosciences Laboratory, Inc.. The 510(k) number is K911559.

When did ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID receive FDA 510(k) clearance?

ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID received FDA 510(k) clearance on 1991-04-22, under 510(k) number K911559.

Who is the listed applicant for ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID?

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

What is the FDA product code for ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID?

The FDA product code for ANTIMICROBIAL SUSCEPT. TEST PANEL CEFONICID is JWY.

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Other records listing Alamar Biosciences Laboratory, 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.

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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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