The following data is part of a premarket notification filed by Pausch Corp. with the FDA for Compact System.
Device ID | K790741 |
510k Number | K790741 |
Device Name: | COMPACT SYSTEM |
Classification | System, X-ray, Stationary |
Applicant | PAUSCH CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KPR |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-04-16 |
Decision Date | 1979-04-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
COMPACT SYSTEM 74034177 not registered Dead/Abandoned |
Daifuku Company Ltd. 1990-03-02 |