The following data is part of a premarket notification filed by Unique Flotation Systems, Inc. with the FDA for Stage Iii.
Device ID | K903659 |
510k Number | K903659 |
Device Name: | STAGE III |
Classification | Bed, Flotation Therapy, Powered |
Applicant | UNIQUE FLOTATION SYSTEMS, INC. 121 ENTERPRISE COURT Corona, CA 91720 |
Contact | Robert J Nangle |
Correspondent | Robert J Nangle UNIQUE FLOTATION SYSTEMS, INC. 121 ENTERPRISE COURT Corona, CA 91720 |
Product Code | IOQ |
CFR Regulation Number | 890.5170 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-09 |
Decision Date | 1990-09-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STAGE III 78227876 not registered Dead/Abandoned |
Stage III Technologies, L.C. 2003-03-20 |
STAGE III 75677370 not registered Dead/Abandoned |
STAGE III TECHNOLOGIES L.C. 1999-04-08 |
STAGE III 74244873 1777646 Dead/Cancelled |
Cooper Industries, Inc. 1992-02-10 |
STAGE III 74244061 1759467 Dead/Cancelled |
Cooper Industries, Inc. 1992-02-07 |
STAGE III 73518463 1351897 Dead/Cancelled |
MILTON BRADLEY COMPANY 1985-01-22 |
STAGE III 73207248 1143787 Dead/Cancelled |
Earcetera, Inc. 1979-03-13 |
STAGE III 73207203 1143306 Dead/Cancelled |
Earcetera, Inc. 1979-03-13 |
STAGE III 73054702 1030240 Dead/Expired |
LIGGETT & MYERS INCORPORATED 1975-06-10 |