The following data is part of a premarket notification filed by Medtrade Products Ltd. with the FDA for Medtrade Products Alginate Island.
Device ID | K000487 |
510k Number | K000487 |
Device Name: | MEDTRADE PRODUCTS ALGINATE ISLAND |
Classification | Dressing, Wound, Collagen |
Applicant | MEDTRADE PRODUCTS LTD. ELECTRA HOUSE CREWE BUSINESS PARK Crewe, Cheshire, GB Cw1 6gl |
Contact | Jonathan Ranfield |
Correspondent | Jonathan Ranfield MEDTRADE PRODUCTS LTD. ELECTRA HOUSE CREWE BUSINESS PARK Crewe, Cheshire, GB Cw1 6gl |
Product Code | KGN |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-02-14 |
Decision Date | 2000-04-18 |