The following data is part of a premarket notification filed by Meda Ltd. with the FDA for Ultrasonic Biometer/ Pachymeter For Ophthalmology, Model Odm 2100, 2200.
Device ID | K063472 |
510k Number | K063472 |
Device Name: | ULTRASONIC BIOMETER/ PACHYMETER FOR OPHTHALMOLOGY, MODEL ODM 2100, 2200 |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | MEDA LTD. 5905 FAWN LN. Cleveland, OH 44141 |
Contact | Edward A Kroll |
Correspondent | Edward A Kroll MEDA LTD. 5905 FAWN LN. Cleveland, OH 44141 |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-11-15 |
Decision Date | 2007-01-31 |
Summary: | summary |