510(k) K935760
K935760 is an FDA 510(k) premarket notification submitted by Medtec, Inc. for the device "TEC 2100 (MODEL MT-LPLGD)". The FDA issued a decision of Substantially Equivalent on January 25, 1994. The device falls under product code IWE (Monitor, Patient Position, Light-Beam), a Class I device regulated under 21 CFR 892.5780. Medtec, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 25, 1994
- Date Received
- November 26, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Monitor, Patient Position, Light-Beam
- Device Class
- Class I
- Regulation Number
- 892.5780
- Review Panel
- RA
- Submission Type