MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE
K-Number: K020939 · 2002-05-17
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Device Summary
Frequently Asked Questions
What is the MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE?
MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE is a medical device that received FDA 510(k) clearance on 2002-05-17. The listed applicant is Dade Microscan, Inc.. The 510(k) number is K020939.
When did MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE receive FDA 510(k) clearance?
MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE received FDA 510(k) clearance on 2002-05-17, under 510(k) number K020939.
Who is the listed applicant for MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE?
The FDA 510(k) record lists Dade Microscan, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE?
The FDA product code for MICROSCAN MICROSTREP PLUS PANEL-TETRACYCLINE is LTT.
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 Dade Microscan, 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: LTT)
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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