The following data is part of a premarket notification filed by Latex Ind., Inc. with the FDA for Catheter, Akron Foley Teflon.
| Device ID | K781751 |
| 510k Number | K781751 |
| Device Name: | CATHETER, AKRON FOLEY TEFLON |
| Classification | Catheter, Urological |
| Applicant | LATEX IND., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOD |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-10-16 |
| Decision Date | 1979-01-22 |