CRAFON ARTHROSCOPY LINES— 510(k) K830673

Substantially Equivalent

Gambro, Inc.

FDA 510(k) clearance K830673 for CRAFON ARTHROSCOPY LINES, Substantially Equivalent on 1983-06-08. Applicant: Gambro, Inc..

Clearance details

Applicant: Gambro, Inc.
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 1983-03-04
Decision date: 1983-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.