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FDA 510(k)

DIASONICS ADA400 ADVANCED DIGITAL ARRAY

K-Number: K851972 · 1985-12-31

ApplicantDiasonics, Inc.
Decision Date1985-12-31
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIASONICS ADA400 ADVANCED DIGITAL ARRAY is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1985-12-31 under 510(k) number K851972. 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 DIASONICS ADA400 ADVANCED DIGITAL ARRAY?

DIASONICS ADA400 ADVANCED DIGITAL ARRAY is a medical device that received FDA 510(k) clearance on 1985-12-31. The listed applicant is Diasonics, Inc.. The 510(k) number is K851972.

When did DIASONICS ADA400 ADVANCED DIGITAL ARRAY receive FDA 510(k) clearance?

DIASONICS ADA400 ADVANCED DIGITAL ARRAY received FDA 510(k) clearance on 1985-12-31, under 510(k) number K851972.

Who is the listed applicant for DIASONICS ADA400 ADVANCED DIGITAL ARRAY?

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 ADA400 ADVANCED DIGITAL ARRAY?

The FDA product code for DIASONICS ADA400 ADVANCED DIGITAL ARRAY 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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