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FDA 510(k)

PIESOMETER, MODEL MK-1

K-Number: K041169 · 2004-08-24

ApplicantCanamet Canadian Natl Medical Technologies, Inc.
Decision Date2004-08-24
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PIESOMETER, MODEL MK-1 is the device name listed in this FDA 510(k) record. The listed applicant is Canamet Canadian Natl Medical Technologies, Inc.. It received FDA 510(k) clearance on 2004-08-24 under 510(k) number K041169. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIESOMETER, MODEL MK-1?

PIESOMETER, MODEL MK-1 is a medical device that received FDA 510(k) clearance on 2004-08-24. The listed applicant is Canamet Canadian Natl Medical Technologies, Inc.. The 510(k) number is K041169.

When did PIESOMETER, MODEL MK-1 receive FDA 510(k) clearance?

PIESOMETER, MODEL MK-1 received FDA 510(k) clearance on 2004-08-24, under 510(k) number K041169.

Who is the listed applicant for PIESOMETER, MODEL MK-1?

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

What is the FDA product code for PIESOMETER, MODEL MK-1?

The FDA product code for PIESOMETER, MODEL MK-1 is DXN.

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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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