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FDA 510(k)

POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A

K-Number: K992886 · 1999-11-09

ApplicantToshiba America Medical Systems, In.C
Decision Date1999-11-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A 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 1999-11-09 under 510(k) number K992886. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A?

POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A is a medical device that received FDA 510(k) clearance on 1999-11-09. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K992886.

When did POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A receive FDA 510(k) clearance?

POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A received FDA 510(k) clearance on 1999-11-09, under 510(k) number K992886.

Who is the listed applicant for POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A?

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 POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A?

The FDA product code for POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A is LLZ.

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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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