NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. DEPOT— 510(k) K870187

Substantially Equivalent

Norfolk Medical Products, Inc.

FDA 510(k) clearance K870187 for NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. DEPOT, Substantially Equivalent on 1987-05-07. Applicant: Norfolk Medical Products, Inc..

Clearance details

Applicant: Norfolk Medical Products, Inc.
Product code: Code LJT
Advisory panel: General Hospital
Date received: 1987-01-16
Decision date: 1987-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skokie, IL, US

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Adverse events under product code LJT

product code LJT

Death: 234
Injury: 6,468
Malfunction: 5,326
Other: 2
Total: 12,030

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.