FDA 510(k)

SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A

K-Number: K960948 · 1996-12-23

Decision Date1996-12-23

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1996-12-23 under 510(k) number K960948. 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 SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A?

SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A is a medical device that received FDA 510(k) clearance on 1996-12-23. The listed applicant is Toshiba Medical Systems. The 510(k) number is K960948.

When did SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A receive FDA 510(k) clearance?

SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A received FDA 510(k) clearance on 1996-12-23, under 510(k) number K960948.

Who is the listed applicant for SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A?

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

What is the FDA product code for SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A?

The FDA product code for SCATTER CORRECTION VOLUME SOFTWARE MODEL NSSC-020A is KPS.

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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.