CABOT FIBER LASER PROBE— 510(k) K873115

Substantially Equivalent

Cabot Medical Corp.

FDA 510(k) clearance K873115 for CABOT FIBER LASER PROBE, Substantially Equivalent on 1988-01-28. Applicant: Cabot Medical Corp..

Clearance details

Applicant: Cabot Medical Corp.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1987-08-10
Decision date: 1988-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Langhorne, PA, US

Download summary PDF View on FDA.gov ↗

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.