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FDA 510(k)

EK/P. AERUGINOSA PNA FISH

K-Number: K092393 · 2009-09-01

ApplicantAdvandx, Inc.
Decision Date2009-09-01
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EK/P. AERUGINOSA PNA FISH is the device name listed in this FDA 510(k) record. The listed applicant is Advandx, Inc.. It received FDA 510(k) clearance on 2009-09-01 under 510(k) number K092393. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EK/P. AERUGINOSA PNA FISH?

EK/P. AERUGINOSA PNA FISH is a medical device that received FDA 510(k) clearance on 2009-09-01. The listed applicant is Advandx, Inc.. The 510(k) number is K092393.

When did EK/P. AERUGINOSA PNA FISH receive FDA 510(k) clearance?

EK/P. AERUGINOSA PNA FISH received FDA 510(k) clearance on 2009-09-01, under 510(k) number K092393.

Who is the listed applicant for EK/P. AERUGINOSA PNA FISH?

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

What is the FDA product code for EK/P. AERUGINOSA PNA FISH?

The FDA product code for EK/P. AERUGINOSA PNA FISH is JSS.

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 Advandx, 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 20 devices →

Related Devices (Code: JSS)

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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