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FDA 510(k)

ADA-1000 (ADVANCED DIGITAL ARRAY)

K-Number: K863780 · 1986-12-29

ApplicantDiasonics, Inc.
Decision Date1986-12-29
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent for Some Indications

Device Summary

ADA-1000 (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 1986-12-29 under 510(k) number K863780. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ADA-1000 (ADVANCED DIGITAL ARRAY)?

ADA-1000 (ADVANCED DIGITAL ARRAY) is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is Diasonics, Inc.. The 510(k) number is K863780.

When did ADA-1000 (ADVANCED DIGITAL ARRAY) receive FDA 510(k) clearance?

ADA-1000 (ADVANCED DIGITAL ARRAY) received FDA 510(k) clearance on 1986-12-29, under 510(k) number K863780.

Who is the listed applicant for ADA-1000 (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 ADA-1000 (ADVANCED DIGITAL ARRAY)?

The FDA product code for ADA-1000 (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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