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 |