510(k) K101892 ยท DXQ Blood Pressure Cuff
HEINE GAMMA G7; HEINE GAMMA G5, HEINE GAMMA GP, HEINE GAMMA GST, HEINE GAMMA XXL LF MODEL M-000.09.23X, M-000.09.24X, M-
| Applicant | Heine Optotechnik GmbH & Co. KG, Hamburg, DE |
| Decision | Substantially Equivalent, Aug 27, 2010 |
| Received | Jul 7, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101892
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.