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FDA 510(k)

DS-7 NUCLEAR MEDICINE GAMMA CAMERA

K-Number: K872297 · 1987-08-12

Decision Date1987-08-12
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DS-7 NUCLEAR MEDICINE GAMMA CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Sopha Medical Systems, Inc.. It received FDA 510(k) clearance on 1987-08-12 under 510(k) number K872297. 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 DS-7 NUCLEAR MEDICINE GAMMA CAMERA?

DS-7 NUCLEAR MEDICINE GAMMA CAMERA is a medical device that received FDA 510(k) clearance on 1987-08-12. The listed applicant is Sopha Medical Systems, Inc.. The 510(k) number is K872297.

When did DS-7 NUCLEAR MEDICINE GAMMA CAMERA receive FDA 510(k) clearance?

DS-7 NUCLEAR MEDICINE GAMMA CAMERA received FDA 510(k) clearance on 1987-08-12, under 510(k) number K872297.

Who is the listed applicant for DS-7 NUCLEAR MEDICINE GAMMA CAMERA?

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

What is the FDA product code for DS-7 NUCLEAR MEDICINE GAMMA CAMERA?

The FDA product code for DS-7 NUCLEAR MEDICINE GAMMA CAMERA is IYX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Sopha Medical Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: IYX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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