The following data is part of a premarket notification filed by Ferris Mfg. Corp. with the FDA for Ferris Polymem Polywic Sterile Cavity Wound Filler.
| Device ID | K990906 |
| 510k Number | K990906 |
| Device Name: | FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER |
| Classification | Bandage, Liquid |
| Applicant | FERRIS MFG. CORP. 16 WEST 300 83RD ST. Burr Ridge, IL 60527 |
| Contact | Theodore R Thorson |
| Correspondent | Theodore R Thorson FERRIS MFG. CORP. 16 WEST 300 83RD ST. Burr Ridge, IL 60527 |
| 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 | 1999-03-18 |
| Decision Date | 1999-04-29 |