The following data is part of a premarket notification filed by Gaymar Industries, Inc. with the FDA for Mul-t-pad.
| Device ID | K832819 |
| 510k Number | K832819 |
| Device Name: | MUL-T-PAD |
| Classification | Pack, Hot Or Cold, Water Circulating |
| Applicant | GAYMAR INDUSTRIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | ILO |
| CFR Regulation Number | 890.5720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-19 |
| Decision Date | 1983-09-26 |