SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS
K-Number: K003834 · 2001-02-23
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Device Summary
Frequently Asked Questions
What is the SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS?
SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS is a medical device that received FDA 510(k) clearance on 2001-02-23. The listed applicant is Trek Diagnostic Systems, Inc.. The 510(k) number is K003834.
When did SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS receive FDA 510(k) clearance?
SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS received FDA 510(k) clearance on 2001-02-23, under 510(k) number K003834.
Who is the listed applicant for SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS?
The FDA 510(k) record lists Trek Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS?
The FDA product code for SENSITITRE SUSCEPTIBILITY PLATES-ADDITIONAL ANTIMICROBICS 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 Trek Diagnostic Systems, 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.
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
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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