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FDA 510(k)

C.P.R. LANDMARC

K-Number: K900415 · 1990-06-12

ApplicantCan-Am Medical, Inc.
Decision Date1990-06-12
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

C.P.R. LANDMARC is the device name listed in this FDA 510(k) record. The listed applicant is Can-Am Medical, Inc.. It received FDA 510(k) clearance on 1990-06-12 under 510(k) number K900415. The device is classified under product code LIX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.P.R. LANDMARC?

C.P.R. LANDMARC is a medical device that received FDA 510(k) clearance on 1990-06-12. The listed applicant is Can-Am Medical, Inc.. The 510(k) number is K900415.

When did C.P.R. LANDMARC receive FDA 510(k) clearance?

C.P.R. LANDMARC received FDA 510(k) clearance on 1990-06-12, under 510(k) number K900415.

Who is the listed applicant for C.P.R. LANDMARC?

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

What is the FDA product code for C.P.R. LANDMARC?

The FDA product code for C.P.R. LANDMARC is LIX.

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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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