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FDA 510(k)

DIASONICS MT/P IMAGING SYSTEM

K-Number: K883516 · 1988-10-07

ApplicantDiasonics, Inc.
Decision Date1988-10-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIASONICS MT/P IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K883516. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIASONICS MT/P IMAGING SYSTEM?

DIASONICS MT/P IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is Diasonics, Inc.. The 510(k) number is K883516.

When did DIASONICS MT/P IMAGING SYSTEM receive FDA 510(k) clearance?

DIASONICS MT/P IMAGING SYSTEM received FDA 510(k) clearance on 1988-10-07, under 510(k) number K883516.

Who is the listed applicant for DIASONICS MT/P IMAGING SYSTEM?

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

What is the FDA product code for DIASONICS MT/P IMAGING SYSTEM?

The FDA product code for DIASONICS MT/P IMAGING SYSTEM is LNH.

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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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