The following data is part of a premarket notification filed by Wfr/aquaplast Corp. with the FDA for Aquaplast.
Device ID | K935067 |
510k Number | K935067 |
Device Name: | AQUAPLAST |
Classification | Accelerator, Linear, Medical |
Applicant | WFR/AQUAPLAST CORP. P.O. BOX 635 Wyckoff, NJ 07481 -0635 |
Contact | John R Kirk |
Correspondent | John R Kirk WFR/AQUAPLAST CORP. P.O. BOX 635 Wyckoff, NJ 07481 -0635 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-20 |
Decision Date | 1994-05-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AQUAPLAST 97652650 not registered Live/Pending |
Techniart Spolka Z.O.O. 2022-10-28 |
AQUAPLAST 78918621 3239437 Dead/Cancelled |
Standard Screen Supply Corp. 2006-06-28 |
AQUAPLAST 76331748 2744140 Dead/Cancelled |
Hi-Gear Products, Inc. 2001-10-29 |
AQUAPLAST 74290876 1762658 Live/Registered |
PERFORMANCE HEALTH HOLDINGS, INC. 1992-07-01 |