The following data is part of a premarket notification filed by Ferris Mfg. Corp. with the FDA for Ferris Hydrophilic Dressing.
| Device ID | K880330 |
| 510k Number | K880330 |
| Device Name: | FERRIS HYDROPHILIC DRESSING |
| Classification | Dressing, Wound, Drug |
| Applicant | FERRIS MFG. CORP. 16W300 83RD ST. Burr Ridge, IL 60527 -5848 |
| Contact | Demetra Lalagos |
| Correspondent | Demetra Lalagos FERRIS MFG. CORP. 16W300 83RD ST. Burr Ridge, IL 60527 -5848 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-01-27 |
| Decision Date | 1988-03-23 |