510(k) K913213 ยท HGI Electrocautery, Gynecologic (And Accessories)
SINGLE USE LEE ELECTRODE
| Applicant | Aspen Laboratories, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Feb 13, 1992 |
| Received | Jul 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913213
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.