Does a Novel Needle Over Catheter Device Improve First Pass Success and Decrease Complications

Emergency Department Patients who were to get intravenous (IV) access through routine medical care will receive it through trademarked catheter via convenience sample. Patient and clinician experience, including adverse events, will be recorded. A standardized data entry sheet will be collected at time of enrollment, and then daily thereafter while the subject has the IV. The data collected will remain anonymous.

Inclusion Criteria i. Any gender, 18 years of age or older ii. Acceptable candidate for an elective PIV as determined by physician. iii. Anticipated admission to inpatient unit. Exclusion Criteria 1. Any gender, \< 18 years old. 2. Requirement for emergent IV placement (patient's condition would be compromised if there is a delay in IV placement); 3. Previous venous grafts or surgery at the target vessel access site; 4. Currently involved in other investigational clinical trials (unless permission is granted by other study Pl) 5. Subjects who are pregnant, planning to become pregnant within 3 months of the procedure, or lactating