510(k) K191559 ยท FEQ Pump, Air, Non-Manual, For Endoscope
AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Aug 1, 2019 |
| Received | Jun 13, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191559
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.