LASEVAC— 510(k) K951490

Name: FDA 510(k) clearance K951490
Creator: U.S. Food and Drug Administration
Published: 1995-06-13

Substantially Equivalent

D.D. Surgical, Inc.

FDA 510(k) clearance K951490 for LASEVAC, Substantially Equivalent on 1995-06-13. Applicant: D.D. Surgical, Inc.. Device class: 2.

Clearance details

Applicant: D.D. Surgical, Inc.
Product code: Code HET
Device class: Class 2
Regulation: 21 CFR 884.1720
Advisory panel: Obstetrics/Gynecology
Date received: 1995-03-31
Decision date: 1995-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Easton, MD, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

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.