The following data is part of a premarket notification filed by Smith & Nephew Medical Ltd. with the FDA for Iodosorb.
Device ID | K190730 |
510k Number | K190730 |
Device Name: | IODOSORB |
Classification | Dressing, Wound, Drug |
Applicant | Smith & Nephew Medical Ltd. 101 Hessle Road Hull East Riding Of Yorkshire, GB Hu3 2bn |
Contact | Meenakshi Gupta |
Correspondent | Ana Castillo Smith & Nephew Medical Ltd. 101 Hessle Road Hull East Riding Of Yorkshire, GB Hu3 2bn |
Product Code | FRO |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | Yes |
Date Received | 2019-03-21 |
Decision Date | 2019-12-20 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
30040565122497 | K190730 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
IODOSORB 74247192 1753193 Live/Registered |
WATER SECURITY CORPORATION 1992-02-19 |
IODOSORB 73246420 1165168 Live/Registered |
Perstorp Aktiebolag 1980-01-16 |