SHARPLAN CO2 LAPAROSCOPIC PROBE MODEL 792 TO 792BX— 510(k) K894066

Name: FDA 510(k) clearance K894066
Creator: U.S. Food and Drug Administration
Published: 1989-08-10

Substantially Equivalent

Sharplan Lasers, Inc.

FDA 510(k) clearance K894066 for SHARPLAN CO2 LAPAROSCOPIC PROBE MODEL 792 TO 792BX, Substantially Equivalent on 1989-08-10. Applicant: Sharplan Lasers, Inc.. Device class: 2.

Clearance details

Applicant: Sharplan Lasers, Inc.
Product code: Code GEX
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1989-06-08
Decision date: 1989-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.