A1CNOW FOR RX HOME USE
K-Number: K020234 · 2002-02-15
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Device Summary
Frequently Asked Questions
What is the A1CNOW FOR RX HOME USE?
A1CNOW FOR RX HOME USE is a medical device that received FDA 510(k) clearance on 2002-02-15. The listed applicant is Metrika, Inc.. The 510(k) number is K020234.
When did A1CNOW FOR RX HOME USE receive FDA 510(k) clearance?
A1CNOW FOR RX HOME USE received FDA 510(k) clearance on 2002-02-15, under 510(k) number K020234.
Who is the listed applicant for A1CNOW FOR RX HOME USE?
The FDA 510(k) record lists Metrika, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A1CNOW FOR RX HOME USE?
The FDA product code for A1CNOW FOR RX HOME USE is LCP.
Other records listing Metrika, 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: LCP)
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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