The following data is part of a premarket notification filed by Ferris Mfg. Corp. with the FDA for Ferris Polymem Hydrophilic Wound Dressing.
| Device ID | K932913 |
| 510k Number | K932913 |
| Device Name: | FERRIS POLYMEM HYDROPHILIC WOUND DRESSING |
| Classification | Bandage, Liquid |
| Applicant | FERRIS MFG. CORP. 16W300 83RD ST. Burr Ridge, IL 60527 -5848 |
| Contact | Jeffrey A Dziura |
| Correspondent | Jeffrey A Dziura FERRIS MFG. CORP. 16W300 83RD ST. Burr Ridge, IL 60527 -5848 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-16 |
| Decision Date | 1994-06-07 |