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FDA 510(k)

TISSUE SPECTROSCOPE

K-Number: K992529 · 2000-11-17

ApplicantVital Medical , Ltd.
Decision Date2000-11-17
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TISSUE SPECTROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Medical , Ltd.. It received FDA 510(k) clearance on 2000-11-17 under 510(k) number K992529. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE SPECTROSCOPE?

TISSUE SPECTROSCOPE is a medical device that received FDA 510(k) clearance on 2000-11-17. The listed applicant is Vital Medical , Ltd.. The 510(k) number is K992529.

When did TISSUE SPECTROSCOPE receive FDA 510(k) clearance?

TISSUE SPECTROSCOPE received FDA 510(k) clearance on 2000-11-17, under 510(k) number K992529.

Who is the listed applicant for TISSUE SPECTROSCOPE?

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

What is the FDA product code for TISSUE SPECTROSCOPE?

The FDA product code for TISSUE SPECTROSCOPE is DPW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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