510(k) K935760

TEC 2100 (MODEL MT-LPLGD) by Medtec, Inc. — Product Code IWE

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