DRI-VENT ARTERIAL BLOOD SAMPLING KIT— 510(k) K883840

Unknown

Concord Laboratories, Inc.

FDA 510(k) clearance K883840 for DRI-VENT ARTERIAL BLOOD SAMPLING KIT, Unknown on 1989-05-16. Applicant: Concord Laboratories, Inc..

Clearance details

Applicant: Concord Laboratories, Inc.
Product code: Code LKB
Advisory panel: Unknown
Date received: 1988-09-12
Decision date: 1989-05-16
Decision: Unknown
Clearance type: Traditional
Location: Keene, NH, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LKB

product code LKB

Other: 2
Total: 2

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.