The following data is part of a premarket notification filed by Medical Solutions, Inc. with the FDA for Temp 3.
Device ID | K012276 |
510k Number | K012276 |
Device Name: | TEMP 3 |
Classification | Warmer, Thermal, Infusion Fluid |
Applicant | MEDICAL SOLUTIONS, INC. 3901 CENTERVIEW DR., SUITE W Chantilly, VA 20151 |
Contact | Bruce Heymann |
Correspondent | Bruce Heymann MEDICAL SOLUTIONS, INC. 3901 CENTERVIEW DR., SUITE W Chantilly, VA 20151 |
Product Code | LGZ |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-07-19 |
Decision Date | 2001-08-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TEMP 3 78641103 3179679 Live/Registered |
Medical Solutions, Inc. 2005-06-01 |