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FDA 510(k)

BODYSCAN

K-Number: K870818 · 1987-03-16

ApplicantSiemens Gammasonics, Inc.
Decision Date1987-03-16
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BODYSCAN is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1987-03-16 under 510(k) number K870818. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODYSCAN?

BODYSCAN is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K870818.

When did BODYSCAN receive FDA 510(k) clearance?

BODYSCAN received FDA 510(k) clearance on 1987-03-16, under 510(k) number K870818.

Who is the listed applicant for BODYSCAN?

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

What is the FDA product code for BODYSCAN?

The FDA product code for BODYSCAN is IYX.

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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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