The following data is part of a premarket notification filed by Squibb & Sons, Inc. with the FDA for Stomahesive Sterile Wafer.
| Device ID | K800750 |
| 510k Number | K800750 |
| Device Name: | STOMAHESIVE STERILE WAFER |
| Classification | Collector, Ostomy |
| Applicant | SQUIBB & SONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EXB |
| CFR Regulation Number | 876.5900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-04-04 |
| Decision Date | 1980-05-08 |