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 |