The following data is part of a premarket notification filed by Norwood Abbey , Ltd. with the FDA for Norwood Abbey Centurion Ses Epikeratome.
Device ID | K051486 |
510k Number | K051486 |
Device Name: | NORWOOD ABBEY CENTURION SES EPIKERATOME |
Classification | Keratome, Ac-powered |
Applicant | NORWOOD ABBEY , LTD. 63 WELLS RD. Chelsea Hgts., Victoria, AU 3196 |
Contact | Paul Clark |
Correspondent | Paul Clark NORWOOD ABBEY , LTD. 63 WELLS RD. Chelsea Hgts., Victoria, AU 3196 |
Product Code | HNO |
CFR Regulation Number | 886.4370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-06-06 |
Decision Date | 2005-07-06 |
Summary: | summary |