Respiration Measured Via End-tidal CO2 and Spirometry Study (RESPI)

To collect respiration data via end-tidal CO2 and spirometry and compare respiration rates measured via the two methods.

This is a non-randomized, data collection study that will enroll up to 50 participants. There will be one study visit per participant and no follow up period.

Inclusion Criteria: * Willing and able to provide informed consent * Age 18 or above * Full time or part time BSC employee * Willing and able to participate in the required testing Exclusion Criteria: * Currently enrolled in another clinical trial that might interfere with data collection or placement of the study system * Subject is pregnant as indicated by subject report * Known allergy or sensitivity to materials used in the study (Neoprene, Nylon) * Any past or current medical event that could represent a risk for the subject to perform the study required activities in the opinion of the investigator