The following data is part of a premarket notification filed by Harry J. Bosworth Co. with the FDA for Porcelit.
| Device ID | K790806 |
| 510k Number | K790806 |
| Device Name: | PORCELIT |
| Classification | Light, Surgical Headlight |
| Applicant | HARRY J. BOSWORTH CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EBA |
| CFR Regulation Number | 872.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-24 |
| Decision Date | 1979-08-03 |