FDA 510(k)

E. CAM COINCIDENCE MODE (CM)

K-Number: K970627 · 1997-09-04

ApplicantSiemens Medical Solutions USA, Inc.

Decision Date1997-09-04

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

E. CAM COINCIDENCE MODE (CM) is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1997-09-04 under 510(k) number K970627. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E. CAM COINCIDENCE MODE (CM)?

E. CAM COINCIDENCE MODE (CM) is a medical device that received FDA 510(k) clearance on 1997-09-04. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K970627.

When did E. CAM COINCIDENCE MODE (CM) receive FDA 510(k) clearance?

E. CAM COINCIDENCE MODE (CM) received FDA 510(k) clearance on 1997-09-04, under 510(k) number K970627.

Who is the listed applicant for E. CAM COINCIDENCE MODE (CM)?

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

What is the FDA product code for E. CAM COINCIDENCE MODE (CM)?

The FDA product code for E. CAM COINCIDENCE MODE (CM) is KPS.

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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.