FDA 510(k)

AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A

K-Number: K992992 · 1999-12-03

ApplicantToshiba America Medical Systems, In.C

Decision Date1999-12-03

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1999-12-03 under 510(k) number K992992. 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 AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A?

AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A is a medical device that received FDA 510(k) clearance on 1999-12-03. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K992992.

When did AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A receive FDA 510(k) clearance?

AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A received FDA 510(k) clearance on 1999-12-03, under 510(k) number K992992.

Who is the listed applicant for AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A?

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

What is the FDA product code for AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A?

The FDA product code for AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A 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.