The following data is part of a premarket notification filed by Medtec, Inc. with the FDA for Acrysteel Blocking Tray.
Device ID | K954705 |
510k Number | K954705 |
Device Name: | ACRYSTEEL BLOCKING TRAY |
Classification | Accelerator, Linear, Medical |
Applicant | MEDTEC, INC. P.O. BOX 487 1401 8TH STREET SOUTH EAST Orange City, IA 51041 -0487 |
Contact | Donald F Riibe |
Correspondent | Donald F Riibe MEDTEC, INC. P.O. BOX 487 1401 8TH STREET SOUTH EAST Orange City, IA 51041 -0487 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-10-12 |
Decision Date | 1996-01-05 |