The following data is part of a premarket notification filed by Burke, Inc. with the FDA for Cold/hot Fluid Radiation Pad Neutech.
Device ID | K893706 |
510k Number | K893706 |
Device Name: | COLD/HOT FLUID RADIATION PAD NEUTECH |
Classification | Pack, Hot Or Cold, Water Circulating |
Applicant | BURKE, INC. 11701 S. BELCHER ROAD, SUITE 119 Largo, FL 34643 |
Contact | Robert Burke |
Correspondent | Robert Burke BURKE, INC. 11701 S. BELCHER ROAD, SUITE 119 Largo, FL 34643 |
Product Code | ILO |
CFR Regulation Number | 890.5720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-05-18 |
Decision Date | 1989-06-22 |