The following data is part of a premarket notification filed by Tri W-g, Inc. with the FDA for Mat Table, 8100 Series Mat Platform.
Device ID | K920585 |
510k Number | K920585 |
Device Name: | MAT TABLE, 8100 SERIES MAT PLATFORM |
Classification | Table, Powered |
Applicant | TRI W-G, INC. P.O. BOX 905 Valley City, ND 58072 |
Contact | David Kesler |
Correspondent | David Kesler TRI W-G, INC. P.O. BOX 905 Valley City, ND 58072 |
Product Code | INQ |
CFR Regulation Number | 890.3760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-02-10 |
Decision Date | 1992-04-07 |