ENZYMUN TEST R T3
K-Number: K896900 · 1990-02-08
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Device Summary
Frequently Asked Questions
What is the ENZYMUN TEST R T3?
ENZYMUN TEST R T3 is a medical device that received FDA 510(k) clearance on 1990-02-08. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K896900.
When did ENZYMUN TEST R T3 receive FDA 510(k) clearance?
ENZYMUN TEST R T3 received FDA 510(k) clearance on 1990-02-08, under 510(k) number K896900.
Who is the listed applicant for ENZYMUN TEST R T3?
The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENZYMUN TEST R T3?
The FDA product code for ENZYMUN TEST R T3 is CDP.
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 Boehringer Mannheim Corp. 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: CDP)
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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