THE BULLION— 510(k) K910757

Substantially Equivalent

Octostop, Inc.

FDA 510(k) clearance K910757 for THE BULLION, Substantially Equivalent on 1991-09-16. Applicant: Octostop, Inc..

Clearance details

Applicant: Octostop, Inc.
Product code: Code KPR
Advisory panel: Radiology
Date received: 1991-01-07
Decision date: 1991-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Qc., CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.