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FDA 510(k)

CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100

K-Number: K992606 · 2000-06-21

ApplicantCanon USA, Inc.
Decision Date2000-06-21
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 2000-06-21 under 510(k) number K992606. The device is classified under product code HLI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100?

CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 is a medical device that received FDA 510(k) clearance on 2000-06-21. The listed applicant is Canon USA, Inc.. The 510(k) number is K992606.

When did CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 receive FDA 510(k) clearance?

CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 received FDA 510(k) clearance on 2000-06-21, under 510(k) number K992606.

Who is the listed applicant for CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100?

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

What is the FDA product code for CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100?

The FDA product code for CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 is HLI.

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Other records listing Canon USA, Inc. as applicant

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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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