FDA 510(k)

SUMMIT NUCLEAR VISION NEUROSPECT

K-Number: K920958 · 1992-08-07

Decision Date1992-08-07

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SUMMIT NUCLEAR VISION NEUROSPECT is the device name listed in this FDA 510(k) record. The listed applicant is Summit Nuclear. It received FDA 510(k) clearance on 1992-08-07 under 510(k) number K920958. 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 SUMMIT NUCLEAR VISION NEUROSPECT?

SUMMIT NUCLEAR VISION NEUROSPECT is a medical device that received FDA 510(k) clearance on 1992-08-07. The listed applicant is Summit Nuclear. The 510(k) number is K920958.

When did SUMMIT NUCLEAR VISION NEUROSPECT receive FDA 510(k) clearance?

SUMMIT NUCLEAR VISION NEUROSPECT received FDA 510(k) clearance on 1992-08-07, under 510(k) number K920958.

Who is the listed applicant for SUMMIT NUCLEAR VISION NEUROSPECT?

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

What is the FDA product code for SUMMIT NUCLEAR VISION NEUROSPECT?

The FDA product code for SUMMIT NUCLEAR VISION NEUROSPECT is KPS.

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Other records listing Summit Nuclear as applicant

K935273VISION FX 40 & 80 SERIES GAMMA CAMERA K935318SUMMIT NUCLEAR VISION FX 20 SERIES GAMMA CAMERA SYSTEMS K922427SUMMIT NUCLEAR VISION 1024RZ GAMMA CAMERA SYSTEM K922426SUMMIT NUCLEAR VISION T-22 GAMMA CAMERA SYSTEM K912573VISION (NUCLEAR MEDICINE COMPUTER)

Related Devices (Code: KPS)

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.