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FDA 510(k)

REEVUE INDIRECT CALORIMETER, MODEL#8100

K-Number: K021490 · 2003-01-02

ApplicantKorr Medical Technologies, Inc.
Decision Date2003-01-02
Product CodeBZL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REEVUE INDIRECT CALORIMETER, MODEL#8100 is the device name listed in this FDA 510(k) record. The listed applicant is Korr Medical Technologies, Inc.. It received FDA 510(k) clearance on 2003-01-02 under 510(k) number K021490. The device is classified under product code BZL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REEVUE INDIRECT CALORIMETER, MODEL#8100?

REEVUE INDIRECT CALORIMETER, MODEL#8100 is a medical device that received FDA 510(k) clearance on 2003-01-02. The listed applicant is Korr Medical Technologies, Inc.. The 510(k) number is K021490.

When did REEVUE INDIRECT CALORIMETER, MODEL#8100 receive FDA 510(k) clearance?

REEVUE INDIRECT CALORIMETER, MODEL#8100 received FDA 510(k) clearance on 2003-01-02, under 510(k) number K021490.

Who is the listed applicant for REEVUE INDIRECT CALORIMETER, MODEL#8100?

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

What is the FDA product code for REEVUE INDIRECT CALORIMETER, MODEL#8100?

The FDA product code for REEVUE INDIRECT CALORIMETER, MODEL#8100 is BZL.

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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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