The following data is part of a premarket notification filed by Burke Neutech, Inc. with the FDA for Lsi6000 Thermal Therapy System.
Device ID | K926151 |
510k Number | K926151 |
Device Name: | LSI6000 THERMAL THERAPY SYSTEM |
Classification | Pack, Hot Or Cold, Water Circulating |
Applicant | BURKE NEUTECH, INC. 11701 S. BELCHER RD. SUITE 119 Largo, FL 34643 -5117 |
Contact | Robert E Burke |
Correspondent | Robert E Burke BURKE NEUTECH, INC. 11701 S. BELCHER RD. SUITE 119 Largo, FL 34643 -5117 |
Product Code | ILO |
CFR Regulation Number | 890.5720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-12-07 |
Decision Date | 1993-05-26 |