IMMULITE HS-TSH
K-Number: K905769 · 1991-01-31
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Device Summary
Frequently Asked Questions
What is the IMMULITE HS-TSH?
IMMULITE HS-TSH is a medical device that received FDA 510(k) clearance on 1991-01-31. The listed applicant is Cirrus Diagnostics, Inc.. The 510(k) number is K905769.
When did IMMULITE HS-TSH receive FDA 510(k) clearance?
IMMULITE HS-TSH received FDA 510(k) clearance on 1991-01-31, under 510(k) number K905769.
Who is the listed applicant for IMMULITE HS-TSH?
The FDA 510(k) record lists Cirrus Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMMULITE HS-TSH?
The FDA product code for IMMULITE HS-TSH is JLW.
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 Cirrus 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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