Clearance Summary
S & W MODEL SW 37 received FDA 510(k) clearance under submission number K830874, sponsored by S & W Enterprises, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1983-04-08.
- Submission: K830874
- Applicant / Sponsor: S & W Enterprises, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3760
- Decision date: 1983-04-08
Classification & Regulation
This clearance is catalogued under FDA product code INQ and 21 CFR 890.3760, within the Physical Medicine review panel as a Class I device.