ACCESS(TM), SOFTWARE RELEASE 4.11P— 510(k) K896637

Name: FDA 510(k) clearance K896637
Creator: U.S. Food and Drug Administration
Published: 1990-01-22

Substantially Equivalent

Diasonics, Inc.

FDA 510(k) clearance K896637 for ACCESS(TM), SOFTWARE RELEASE 4.11P, Substantially Equivalent on 1990-01-22. Applicant: Diasonics, Inc.. Device class: 2.

Clearance details

Applicant: Diasonics, Inc.
Product code: Code LPH
Device class: Class 2
Regulation: 21 CFR 888.3358
Advisory panel: Orthopedic
Date received: 1989-11-24
Decision date: 1990-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: S. San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LPH

product code LPH

Death: 73
Injury: 31,640
Malfunction: 3,358
Other: 2
Total: 35,073

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.