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FDA 510(k)

SCANVIEW, MODEL SC-300

K-Number: K071398 · 2007-10-04

ApplicantApplied Spectral Imaging , Ltd.
Decision Date2007-10-04
Product CodeJOY
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SCANVIEW, MODEL SC-300 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Spectral Imaging , Ltd.. It received FDA 510(k) clearance on 2007-10-04 under 510(k) number K071398. The device is classified under product code JOY. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANVIEW, MODEL SC-300?

SCANVIEW, MODEL SC-300 is a medical device that received FDA 510(k) clearance on 2007-10-04. The listed applicant is Applied Spectral Imaging , Ltd.. The 510(k) number is K071398.

When did SCANVIEW, MODEL SC-300 receive FDA 510(k) clearance?

SCANVIEW, MODEL SC-300 received FDA 510(k) clearance on 2007-10-04, under 510(k) number K071398.

Who is the listed applicant for SCANVIEW, MODEL SC-300?

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

What is the FDA product code for SCANVIEW, MODEL SC-300?

The FDA product code for SCANVIEW, MODEL SC-300 is JOY.

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Other records listing Applied Spectral Imaging , Ltd. 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.

K122554GENASIS SCANVIEW SYSTEMK101291SCANVIEW HER2/NEU FISH SYSTEMK050236FISHVIEWK012103BANDVIEW SYSTEMK973950RETINAL CUBE

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Official Source

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