The following data is part of a premarket notification filed by Apple Medical Corp. with the FDA for The Assistant.
Device ID | K952841 |
510k Number | K952841 |
Device Name: | THE ASSISTANT |
Classification | Clamp, Penile |
Applicant | APPLE MEDICAL CORP. 580 MAIN ST. Bolton, MA 01740 |
Contact | Scott E Coleridge |
Correspondent | Scott E Coleridge APPLE MEDICAL CORP. 580 MAIN ST. Bolton, MA 01740 |
Product Code | FHA |
CFR Regulation Number | 876.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-21 |
Decision Date | 1995-08-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
THE ASSISTANT 90687135 not registered Live/Pending |
RK Solutions, LLC 2021-05-03 |
THE ASSISTANT 87583722 5613090 Live/Registered |
Scentsible, LLC 2017-08-25 |
THE ASSISTANT 86868259 5103359 Live/Registered |
Quick Workz, LLC 2016-01-07 |
THE ASSISTANT 78426379 3249951 Dead/Cancelled |
VIACOM INTERNATIONAL INC. 2004-05-27 |
THE ASSISTANT 76129707 2482427 Dead/Cancelled |
Kinematics, Inc. 2000-09-18 |
THE ASSISTANT 75652422 not registered Dead/Abandoned |
Kinematics, Inc. 1999-03-03 |
THE ASSISTANT 73805181 not registered Dead/Abandoned |
RXCLINICAL INC. 1989-06-07 |