ORTHO RECOMBIPLASTIN II W/ORTHO RECOMBIPLASTIN II DILUENT— 510(k) K935748

Substantially Equivalent

Ortho Diagnostic Systems, Inc.

FDA 510(k) clearance K935748 for ORTHO RECOMBIPLASTIN II W/ORTHO RECOMBIPLASTIN II DILUENT, Substantially Equivalent on 1995-04-26. Applicant: Ortho Diagnostic Systems, Inc..

Clearance details

Applicant: Ortho Diagnostic Systems, Inc.
Product code: Code GJS
Advisory panel: Hematology
Date received: 1993-12-01
Decision date: 1995-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raritan, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GJS

product code GJS

Death: 4
Injury: 229
Malfunction: 4,852
Total: 5,085

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.