The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Castle(r) 2510 & 2610 Minor Surg. Light.
| Device ID | K820681 |
| 510k Number | K820681 |
| Device Name: | CASTLE(R) 2510 & 2610 MINOR SURG. LIGHT |
| Classification | Light, Surgical, Ceiling Mounted |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FSY |
| CFR Regulation Number | 878.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-11 |
| Decision Date | 1982-04-15 |