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FDA 510(k)

ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL.

K-Number: K911555 · 1991-04-22

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

Device Summary

ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL. 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 K911555. 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 ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL.?

ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL. 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 K911555.

When did ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL. receive FDA 510(k) clearance?

ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL. received FDA 510(k) clearance on 1991-04-22, under 510(k) number K911555.

Who is the listed applicant for ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL.?

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 ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL.?

The FDA product code for ANITIMICROBIAL SUSCEPT. TEST PANEL AMOX./CLAVUL. is JWY.

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Other records listing Alamar Biosciences Laboratory, Inc. as applicant

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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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