The following data is part of a premarket notification filed by Solace Therapeutics with the FDA for Guardian Urethral Sheath.
Device ID | K141252 |
510k Number | K141252 |
Device Name: | GUARDIAN URETHRAL SHEATH |
Classification | Accessories, Catheter, G-u |
Applicant | SOLACE THERAPEUTICS 135 NEWBURY ST Framingham, MA 01701 |
Contact | Adam Heroux |
Correspondent | Adam Heroux SOLACE THERAPEUTICS 135 NEWBURY ST Framingham, MA 01701 |
Product Code | KNY |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-05-14 |
Decision Date | 2014-06-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GUARDIAN URETHRAL SHEATH 86238493 4624978 Live/Registered |
Solace Therapeutics, Inc. 2014-04-01 |