IV HOUSE— 510(k) K912942

Substantially Equivalent

Progressive Iv'S, Inc.

FDA 510(k) clearance K912942 for IV HOUSE, Substantially Equivalent on 1991-09-25. Applicant: Progressive Iv'S, Inc..

Clearance details

Applicant: Progressive Iv'S, Inc.
Product code: Code KMK
Advisory panel: General Hospital
Date received: 1991-07-03
Decision date: 1991-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hazelwood, MO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KMK

product code KMK

Malfunction: 461
Other: 1
Total: 462

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.