The following data is part of a premarket notification filed by Escalon Medical Corp. with the FDA for Vascuview Tap Ultrasound System.
Device ID | K093613 |
510k Number | K093613 |
Device Name: | VASCUVIEW TAP ULTRASOUND SYSTEM |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | ESCALON MEDICAL CORP. 2440 SOUTH 179TH ST. New Berlin, WI 53146 |
Contact | Roger Edens |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | IYN |
Subsequent Product Code | ITX |
Subsequent Product Code | IYO |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2009-11-23 |
Decision Date | 2009-12-23 |
Summary: | summary |