Clearance Summary
DUKKI received FDA 510(k) clearance under submission number K913544, sponsored by Pin Dot Products, 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 1991-08-29.
- Submission: K913544
- Applicant / Sponsor: Pin Dot Products, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3100
- Decision date: 1991-08-29
Classification & Regulation
This clearance is catalogued under FDA product code INM and 21 CFR 890.3100, within the Physical Medicine review panel as a Class I device.