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FDA 510(k)

SCANVIEW SYSTEM

K-Number: K110345 · 2011-10-19

ApplicantApplied Spectral Imaging
Decision Date2011-10-19
Product CodeNTH
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

SCANVIEW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Applied Spectral Imaging. It received FDA 510(k) clearance on 2011-10-19 under 510(k) number K110345. The device is classified under product code NTH. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANVIEW SYSTEM?

SCANVIEW SYSTEM is a medical device that received FDA 510(k) clearance on 2011-10-19. The listed applicant is Applied Spectral Imaging. The 510(k) number is K110345.

When did SCANVIEW SYSTEM receive FDA 510(k) clearance?

SCANVIEW SYSTEM received FDA 510(k) clearance on 2011-10-19, under 510(k) number K110345.

Who is the listed applicant for SCANVIEW SYSTEM?

The FDA 510(k) record lists Applied Spectral Imaging as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCANVIEW SYSTEM?

The FDA product code for SCANVIEW SYSTEM is NTH.

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Related Devices (Code: NTH)

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

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