510(k) K930842 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
| Applicant | Grieshaber & Co., Kennesaw GA, US |
| Decision | Substantially Equivalent, May 3, 1994 |
| Received | Feb 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930842
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.