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FDA 510(k)

A1CNOW FOR HOME USE

K-Number: K022661 · 2002-12-13

ApplicantMetrika, Inc.
Decision Date2002-12-13
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

A1CNOW FOR HOME USE is the device name listed in this FDA 510(k) record. The listed applicant is Metrika, Inc.. It received FDA 510(k) clearance on 2002-12-13 under 510(k) number K022661. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A1CNOW FOR HOME USE?

A1CNOW FOR HOME USE is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Metrika, Inc.. The 510(k) number is K022661.

When did A1CNOW FOR HOME USE receive FDA 510(k) clearance?

A1CNOW FOR HOME USE received FDA 510(k) clearance on 2002-12-13, under 510(k) number K022661.

Who is the listed applicant for A1CNOW FOR 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 HOME USE?

The FDA product code for A1CNOW FOR 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.

View all 11 devices →

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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