Clearance Summary
PULSE GENERATOR, MODEL 240, EXTERNAL received FDA 510(k) clearance under submission number K781327, sponsored by Intermedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1978-12-11.
- Submission: K781327
- Applicant / Sponsor: Intermedics, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3600
- Decision date: 1978-12-11
Classification & Regulation
This clearance is catalogued under FDA product code DTE and 21 CFR 870.3600, within the Cardiovascular review panel as a Class II device.