The following data is part of a premarket notification filed by Orthopedic Equipment Co., Inc. with the FDA for Toe Loops.
Device ID | K780194 |
510k Number | K780194 |
Device Name: | TOE LOOPS |
Classification | Accessories, Wheelchair |
Applicant | ORTHOPEDIC EQUIPMENT CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KNO |
CFR Regulation Number | 890.3910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-02-03 |
Decision Date | 1978-02-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TOE LOOPS 87730307 5534430 Live/Registered |
3-Point Products, Inc. 2017-12-21 |
TOE LOOPS 78875786 3367392 Dead/Cancelled |
3 Point Products, Inc. 2006-05-03 |