BETA-TSH-IRMA
K-Number: K853977 · 1985-10-22
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Device Summary
Frequently Asked Questions
What is the BETA-TSH-IRMA?
BETA-TSH-IRMA is a medical device that received FDA 510(k) clearance on 1985-10-22. The listed applicant is Leeco Diagnostics, Inc.. The 510(k) number is K853977.
When did BETA-TSH-IRMA receive FDA 510(k) clearance?
BETA-TSH-IRMA received FDA 510(k) clearance on 1985-10-22, under 510(k) number K853977.
Who is the listed applicant for BETA-TSH-IRMA?
The FDA 510(k) record lists Leeco Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BETA-TSH-IRMA?
The FDA product code for BETA-TSH-IRMA is JLW.
Other records listing Leeco Diagnostics, 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: JLW)
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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