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FDA 510(k)

INVIEW

K-Number: K051321 · 2005-06-13

ApplicantMetrika, Inc.
Decision Date2005-06-13
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

INVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Metrika, Inc.. It received FDA 510(k) clearance on 2005-06-13 under 510(k) number K051321. 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 INVIEW?

INVIEW is a medical device that received FDA 510(k) clearance on 2005-06-13. The listed applicant is Metrika, Inc.. The 510(k) number is K051321.

When did INVIEW receive FDA 510(k) clearance?

INVIEW received FDA 510(k) clearance on 2005-06-13, under 510(k) number K051321.

Who is the listed applicant for INVIEW?

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 INVIEW?

The FDA product code for INVIEW is LCP.

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Other records listing Metrika, Inc. as applicant

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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.

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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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