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FDA 510(k)

MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM

K-Number: K930579 · 1993-11-03

ApplicantMedison America, Inc.
Decision Date1993-11-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medison America, Inc.. It received FDA 510(k) clearance on 1993-11-03 under 510(k) number K930579. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM?

MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM is a medical device that received FDA 510(k) clearance on 1993-11-03. The listed applicant is Medison America, Inc.. The 510(k) number is K930579.

When did MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM receive FDA 510(k) clearance?

MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM received FDA 510(k) clearance on 1993-11-03, under 510(k) number K930579.

Who is the listed applicant for MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM?

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

What is the FDA product code for MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM?

The FDA product code for MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM is IYO.

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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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