510(k) K982706— PHILIPS BV300 SERIES RELEASE 2.1

Substantially Equivalent

Philips Medical Systems, Inc.

Clearance details

Applicant: Philips Medical Systems, Inc.
Product code: Code OXO
Advisory panel: Radiology
Date received: 1998-08-04
Decision date: 1998-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shelton, CT, US

Adverse events under product code OXO

product code OXO

Death: 6
Injury: 163
Malfunction: 2,099
Other: 1
Total: 2,269

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.