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FDA 510(k)

ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS

K-Number: K904689 · 1991-02-07

Decision Date1991-02-07
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS 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 1991-02-07 under 510(k) number K904689. 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/ADD ANTIBIOTICS?

ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS is a medical device that received FDA 510(k) clearance on 1991-02-07. The listed applicant is Alamar Biosciences Laboratory, Inc.. The 510(k) number is K904689.

When did ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS receive FDA 510(k) clearance?

ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS received FDA 510(k) clearance on 1991-02-07, under 510(k) number K904689.

Who is the listed applicant for ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS?

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/ADD ANTIBIOTICS?

The FDA product code for ANTIMICROBIAL SUSCEPT TEST PANEL/ADD ANTIBIOTICS is JWY.

Related Clinical Trials

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.

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.

View all 26 devices →

Related Devices (Code: JWY)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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