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 |