The following data is part of a premarket notification filed by Medical Products Development, Inc. with the FDA for Hi-temp Looptip Surgical Cautery.
| Device ID | K802330 |
| 510k Number | K802330 |
| Device Name: | HI-TEMP LOOPTIP SURGICAL CAUTERY |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | MEDICAL PRODUCTS DEVELOPMENT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-23 |
| Decision Date | 1980-11-12 |