The following data is part of a premarket notification filed by Valmed, Inc. with the FDA for Valu-plus Pad.
Device ID | K925336 |
510k Number | K925336 |
Device Name: | VALU-PLUS PAD |
Classification | Components, Wheelchair |
Applicant | VALMED, INC. 931 DANIEL ST. POST OFFICE BOX 698 NEW ORLEANS, LA 70063 |
Contact | WILLIAM C MAIN |
Correspondent | WILLIAM C MAIN VALMED, INC. 931 DANIEL ST. POST OFFICE BOX 698 NEW ORLEANS, LA 70063 |
Product Code | KNN |
CFR Regulation Number | 890.3920 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-10-22 |
Decision Date | 1993-02-12 |