The following data is part of a premarket notification filed by Orange-sol, Inc. with the FDA for Medi-sol.
Device ID | K924571 |
510k Number | K924571 |
Device Name: | MEDI-SOL |
Classification | Solvent, Adhesive Tape |
Applicant | ORANGE-SOL, INC. 955 N. FIESTA BLVD., STE. #1 Gilbert, AZ 85234 |
Contact | Gurney |
Correspondent | Gurney ORANGE-SOL, INC. 955 N. FIESTA BLVD., STE. #1 Gilbert, AZ 85234 |
Product Code | KOX |
CFR Regulation Number | 878.4730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-10 |
Decision Date | 1993-04-06 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEDI-SOL 76567224 2912553 Live/Registered |
THE ORANGE-SOL GROUP OF COMPANIES, LTD. 2003-12-24 |
MEDI-SOL 73757093 1589605 Dead/Cancelled |
ORANGE-SOL, INC. 1988-10-05 |