The following data is part of a premarket notification filed by Lorvic Corp. with the FDA for U. V. Germicidal Unit.
| Device ID | K871615 |
| 510k Number | K871615 |
| Device Name: | U. V. GERMICIDAL UNIT |
| Classification | Sterilizer, Dry Heat |
| Applicant | LORVIC CORP. 8810 FROST AVE. St. Louis, MO 63134 |
| Contact | John M Barrett |
| Correspondent | John M Barrett LORVIC CORP. 8810 FROST AVE. St. Louis, MO 63134 |
| Product Code | KMH |
| CFR Regulation Number | 880.6870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-04-27 |
| Decision Date | 1987-09-11 |