ARAGON SURGICAL LAPCAP— 510(k) K070651

Name: FDA 510(k) clearance K070651
Creator: U.S. Food and Drug Administration
Published: 2007-05-30

Substantially Equivalent

Aragon Surgical, Inc.

FDA 510(k) clearance K070651 for ARAGON SURGICAL LAPCAP, Substantially Equivalent on 2007-05-30. Applicant: Aragon Surgical, Inc.. Device class: 2.

Clearance details

Applicant: Aragon Surgical, Inc.
Product code: Code HIF
Device class: Class 2
Regulation: 21 CFR 884.1730
Advisory panel: Obstetrics/Gynecology
Date received: 2007-03-09
Decision date: 2007-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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K081312 — ARAGON ONESHOT SYSTEM2008-10-31
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Adverse events under product code HIF

product code HIF

Death: 19
Injury: 578
Malfunction: 5,639
Total: 6,236

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.