The following data is part of a premarket notification filed by Oculus Innovative Sciences, Inc. with the FDA for Pediacyn Atopic Dermatitis Hydrogel.
| Device ID | K102945 |
| 510k Number | K102945 |
| Device Name: | PEDIACYN ATOPIC DERMATITIS HYDROGEL |
| Classification | Dressing, Wound, Drug |
| Applicant | OCULUS INNOVATIVE SCIENCES, INC. 1135 N. MC DOWELL BLVD Petaluma, CA 94954 |
| Contact | Antoinette Douglas |
| Correspondent | Antoinette Douglas OCULUS INNOVATIVE SCIENCES, INC. 1135 N. MC DOWELL BLVD Petaluma, CA 94954 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-04 |
| Decision Date | 2011-02-02 |
| Summary: | summary |