510(k) K203060 ยท HQC Unit, Phacofragmentation
VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control
| Applicant | Johnson & Johnson Surgical Vision, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Mar 12, 2021 |
| Received | Oct 8, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203060
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 28, 2023 | Johnson & Johnson Surgical Vision, Inc. VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF) Open, Classified |
HQC | None listed |
| Jan 20, 2023 | Johnson & Johnson Surgical Vision, Inc. Veritas Advanced Infusion Packs, REF: VRT-AI Open, Classified |
HQC | None listed |
| Oct 12, 2022 | Johnson & Johnson Surgical Vision, Inc. Veritas Advanced Infusion Packs. Used in ophthalmic procedures. Open, Classified |
HQC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.