510(k) K083322 ยท GWL Amplifier, Physiological Signal
NEUROMETRIX BIOAMPLIFIER
| Applicant | Neurometrix, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, May 27, 2009 |
| Received | Nov 12, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083322
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.