AVI MICRO 210CM INFUSION PUMP— 510(k) K897013

Substantially Equivalent

3M Company

FDA 510(k) clearance K897013 for AVI MICRO 210CM INFUSION PUMP, Substantially Equivalent on 1990-03-08. Applicant: 3M Company.

Clearance details

Applicant: 3M Company
Product code: Code FRN
Advisory panel: General Hospital
Date received: 1989-12-19
Decision date: 1990-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, 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.