The following data is part of a premarket notification filed by Btl Industries, Inc. with the FDA for Btl-703.
Device ID | K182363 |
510k Number | K182363 |
Device Name: | BTL-703 |
Classification | Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat |
Applicant | BTL Industries, Inc. 362 Elm Street Marlborough, MA 01752 |
Contact | David Chmel |
Correspondent | David Chmel BTL Industries, Inc. 362 Elm Street Marlborough, MA 01752 |
Product Code | IMJ |
CFR Regulation Number | 890.5290 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-30 |
Decision Date | 2019-01-24 |
Summary: | summary |