The following data is part of a premarket notification filed by Ferris Mfg. Corp. with the FDA for Dynafilm.
| Device ID | K874478 |
| 510k Number | K874478 |
| Device Name: | DYNAFILM |
| Classification | Dressing, Wound, Drug |
| Applicant | FERRIS MFG. CORP. 16W300 83RD ST. Burr Ridge, IL 60527 -5848 |
| Contact | Lalagos |
| Correspondent | 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 | 1987-11-02 |
| Decision Date | 1988-01-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DYNAFILM 73341003 1220035 Dead/Cancelled |
National Distillers and Chemical Corporation 1981-12-10 |
![]() DYNAFILM 72116552 0726860 Dead/Expired |
NATIONAL DISTILLERS AND CHEMICAL CORPORATION 1961-03-27 |
![]() DYNAFILM 72116551 0722440 Dead/Cancelled |
National Distillers and Chemical Corporation 1961-03-27 |