SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES
K-Number: K073424 · 2008-01-22
Advertisement
Device Summary
Frequently Asked Questions
What is the SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES?
SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES is a medical device that received FDA 510(k) clearance on 2008-01-22. The listed applicant is Trek Diagnostic Systems, Inc.. The 510(k) number is K073424.
When did SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES receive FDA 510(k) clearance?
SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES received FDA 510(k) clearance on 2008-01-22, under 510(k) number K073424.
Who is the listed applicant for SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES?
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 18-24 HOUR SUSCEPTIBILITY PLATES?
The FDA product code for SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATES 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.
Advertisement