The following data is part of a premarket notification filed by Bioscan, Inc. with the FDA for Light Patch.
| Device ID | K993686 |
| 510k Number | K993686 |
| Device Name: | LIGHT PATCH |
| Classification | Lamp, Infrared, Therapeutic Heating |
| Applicant | BIOSCAN, INC. 6 WALDEN RD. Corrales, NM 87048 |
| Contact | Butch Smith |
| Correspondent | Butch Smith BIOSCAN, INC. 6 WALDEN RD. Corrales, NM 87048 |
| Product Code | ILY |
| CFR Regulation Number | 890.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-01 |
| Decision Date | 2000-07-18 |