I.V. PRO— 510(k) K924180

Substantially Equivalent

I.V. - Pro Tek, Inc.

FDA 510(k) clearance K924180 for I.V. PRO, Substantially Equivalent on 1993-03-16. Applicant: I.V. - Pro Tek, Inc..

Clearance details

Applicant: I.V. - Pro Tek, Inc.
Product code: Code KMK
Advisory panel: General Hospital
Date received: 1992-08-19
Decision date: 1993-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seabrook, TX, US

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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.