The following data is part of a premarket notification filed by Pie Data Medical Bv with the FDA for Ultrasound Linear/sector Scanner 1100.
Device ID | K870653 |
510k Number | K870653 |
Device Name: | ULTRASOUND LINEAR/SECTOR SCANNER 1100 |
Classification | Monitor, Ultrasonic, Fetal |
Applicant | PIE DATA MEDICAL BV PHILIPSWEG 1 Maastricht 6227 Aj, NL |
Contact | Peter Rikers |
Correspondent | Peter Rikers PIE DATA MEDICAL BV PHILIPSWEG 1 Maastricht 6227 Aj, NL |
Product Code | KNG |
CFR Regulation Number | 884.2660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-02-17 |
Decision Date | 1988-02-02 |