The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Castle & Ritter Minor Surg. & Exam Lt.
| Device ID | K811728 |
| 510k Number | K811728 |
| Device Name: | CASTLE & RITTER MINOR SURG. & EXAM LT |
| Classification | Lamp, Surgical |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FTD |
| CFR Regulation Number | 878.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-18 |
| Decision Date | 1981-07-20 |