510(k) K132272 ยท NBW System, Test, Blood Glucose, Over The Counter
GLOOKO DEVICE SYSTEM FOR GLOOKO APPLICATION
| Applicant | Glooko, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Oct 17, 2013 |
| Received | Jul 22, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132272
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.