The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Castle Procedure And Ritter Exam. Tables.
| Device ID | K810900 |
| 510k Number | K810900 |
| Device Name: | CASTLE PROCEDURE AND RITTER EXAM. TABLES |
| Classification | Table, Examination, Medical, Powered |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LGX |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-04-03 |
| Decision Date | 1981-04-21 |