MD2 PERSONAL INFUSION SYSTEM— 510(k) K896544

Substantially Equivalent

Norfolk Medical Products, Inc.

FDA 510(k) clearance K896544 for MD2 PERSONAL INFUSION SYSTEM, Substantially Equivalent on 1990-05-02. Applicant: Norfolk Medical Products, Inc..

Clearance details

Applicant: Norfolk Medical Products, Inc.
Product code: Code FRN
Advisory panel: General Hospital
Date received: 1989-11-17
Decision date: 1990-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skokie, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FRN

product code FRN

Death: 540
Injury: 6,178
Malfunction: 1,464,165
Other: 52
Total: 1,470,935

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.