The following data is part of a premarket notification filed by Surgical Technologies, Inc. with the FDA for Aspirating Endo Ocular Probe.
| Device ID | K930123 |
| 510k Number | K930123 |
| Device Name: | ASPIRATING ENDO OCULAR PROBE |
| Classification | Source, Carrier, Fiberoptic Light |
| Applicant | SURGICAL TECHNOLOGIES, INC. 750 GODDARD AVE. Chesterfield, MO 63005 |
| Contact | Alan T Beckman |
| Correspondent | Alan T Beckman SURGICAL TECHNOLOGIES, INC. 750 GODDARD AVE. Chesterfield, MO 63005 |
| Product Code | EQH |
| CFR Regulation Number | 874.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-12 |
| Decision Date | 1994-02-16 |