The following data is part of a premarket notification filed by Meda Co. Ltd. with the FDA for Ultrasonic Biometer For Ophthalmology Ultrasonic Pachymeter.
Device ID | K121243 |
510k Number | K121243 |
Device Name: | ULTRASONIC BIOMETER FOR OPHTHALMOLOGY ULTRASONIC PACHYMETER |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | MEDA CO. LTD. 13505 BROADFIELD DR. Potomac, MD 20854 |
Contact | Kai Chen |
Correspondent | Kai Chen MEDA CO. LTD. 13505 BROADFIELD DR. Potomac, MD 20854 |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-04-25 |
Decision Date | 2013-05-03 |
Summary: | summary |