CRITIC-ARS
K-Number: K844709 · 1985-01-08
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Device Summary
Frequently Asked Questions
What is the CRITIC-ARS?
CRITIC-ARS is a medical device that received FDA 510(k) clearance on 1985-01-08. The listed applicant is Dimension Diagnostics. The 510(k) number is K844709.
When did CRITIC-ARS receive FDA 510(k) clearance?
CRITIC-ARS received FDA 510(k) clearance on 1985-01-08, under 510(k) number K844709.
Who is the listed applicant for CRITIC-ARS?
The FDA 510(k) record lists Dimension Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRITIC-ARS?
The FDA product code for CRITIC-ARS is JIX.
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 Dimension Diagnostics 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: JIX)
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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