The following data is part of a premarket notification filed by Beecher Medical Diagnostic Instrumentation with the FDA for Beecher 20 Ga. Probe.
| Device ID | K833800 |
| 510k Number | K833800 |
| Device Name: | BEECHER 20 GA. PROBE |
| Classification | Unit, Phacofragmentation |
| Applicant | BEECHER MEDICAL DIAGNOSTIC INSTRUMENTATION 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HQC |
| CFR Regulation Number | 886.4670 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-31 |
| Decision Date | 1984-01-04 |