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FDA 510(k)

DIASONICS DLA-100

K-Number: K833667 · 1984-05-09

ApplicantDiasonics, Inc.
Decision Date1984-05-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIASONICS DLA-100 is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K833667. 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 DLA-100?

DIASONICS DLA-100 is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Diasonics, Inc.. The 510(k) number is K833667.

When did DIASONICS DLA-100 receive FDA 510(k) clearance?

DIASONICS DLA-100 received FDA 510(k) clearance on 1984-05-09, under 510(k) number K833667.

Who is the listed applicant for DIASONICS DLA-100?

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 DLA-100?

The FDA product code for DIASONICS DLA-100 is IYO.

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Other records listing Diasonics, Inc. as applicant

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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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