The following data is part of a premarket notification filed by Medical Products Development, Inc. with the FDA for Perfectemp Ophthalmic Cautery.
| Device ID | K801078 |
| 510k Number | K801078 |
| Device Name: | PERFECTEMP OPHTHALMIC CAUTERY |
| Classification | Unit, Cautery, Thermal, Battery-powered |
| Applicant | MEDICAL PRODUCTS DEVELOPMENT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HQP |
| CFR Regulation Number | 886.4115 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-05-07 |
| Decision Date | 1980-06-04 |