The following data is part of a premarket notification filed by Eastman Kodak Company with the FDA for Kodak T-mat H Film So-118.
| Device ID | K843148 |
| 510k Number | K843148 |
| Device Name: | KODAK T-MAT H FILM SO-118 |
| Classification | Tissue Graft Of Less Than 6mm |
| Applicant | EASTMAN KODAK COMPANY 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | LWZ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-08-10 |
| Decision Date | 1984-08-27 |