PERCUGLIDE— 510(k) K960917

Name: FDA 510(k) clearance K960917
Creator: U.S. Food and Drug Administration
Published: 1996-07-02

Substantially Equivalent

Scientific Device Manufacturer, LLC

FDA 510(k) clearance K960917 for PERCUGLIDE, Substantially Equivalent on 1996-07-02. Applicant: Scientific Device Manufacturer, LLC. Device class: 2.

Clearance details

Applicant: Scientific Device Manufacturer, LLC
Product code: Code DRE
Device class: Class 2
Regulation: 21 CFR 870.1310
Advisory panel: Cardiovascular
Date received: 1996-03-06
Decision date: 1996-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Rafael, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DRE

product code DRE

Death: 100
Injury: 832
Malfunction: 597
Other: 3
Total: 1,532

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.