I.V. START KIT (AHC-50-54954— 510(k) K924192

Unknown

American Healthcare Corp.

FDA 510(k) clearance K924192 for I.V. START KIT (AHC-50-54954, Unknown on 1993-08-27. Applicant: American Healthcare Corp..

Clearance details

Applicant: American Healthcare Corp.
Product code: Code KGX
Advisory panel: General Hospital
Date received: 1992-08-20
Decision date: 1993-08-27
Decision: Unknown
Clearance type: Traditional
Location: South Plainfield, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KGX

product code KGX

Injury: 1,590
Malfunction: 1,357
Other: 3
Total: 2,950

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.