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FDA 510(k)

COLLIMATOR, HEART CONTOUR

K-Number: K781984 · 1978-12-04

ApplicantSiemens Corp.
Decision Date1978-12-04
Product CodeKPW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMATOR, HEART CONTOUR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781984. The device is classified under product code KPW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIMATOR, HEART CONTOUR?

COLLIMATOR, HEART CONTOUR is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Siemens Corp.. The 510(k) number is K781984.

When did COLLIMATOR, HEART CONTOUR receive FDA 510(k) clearance?

COLLIMATOR, HEART CONTOUR received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781984.

Who is the listed applicant for COLLIMATOR, HEART CONTOUR?

The FDA 510(k) record lists Siemens Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLLIMATOR, HEART CONTOUR?

The FDA product code for COLLIMATOR, HEART CONTOUR is KPW.

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Related Devices (Code: KPW)

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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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