Clearance Summary
S/D 600 SPHYGMOMANOMETER AND PULSEMETER received FDA 510(k) clearance under submission number K780805, sponsored by G & W Applied Science Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1978-06-06.
- Submission: K780805
- Applicant / Sponsor: G & W Applied Science Laboratories
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 1978-06-06
Classification & Regulation
This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.