Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Neurovision Medical Products, Inc. · Predicate Candidate Screening
9 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
109 daysmedian FDA review time
357 days90th percentile
9clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K130570 | NEUROVISION MEDICAL MOTION SENSOR | Neurovision Medical Products, Inc. | 2013-12-26 | 297 | 0 |
| K130806 | NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE | Neurovision Medical Products, Inc. | 2013-07-12 | 109 | 0 |
| K113771 | SIGNAL GEAR URETHRAL CATHETER ELECTRODE | Neurovision Medical Products, Inc. | 2012-12-13 | 357 | 0 |
| K121931 | NONDISPOSABLE STIMULATING INSTRUMENTS | Neurovision Medical Products, Inc. | 2012-10-19 | 109 | 0 |
| K110989 | NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE | Neurovision Medical Products, Inc. | 2011-11-03 | 209 | 1 |
| K110140 | NEUROVISION NERVE LOCATOR MONITOR | Neurovision Medical Products, Inc. | 2011-09-30 | 255 | 0 |
| K110712 | DRYTOUCH SUCTION STIMULATOR PROBE | Neurovision Medical Products, Inc. | 2011-06-28 | 106 | 0 |
| K110138 | PAIRED HYDROGEL ELECTRODE | Neurovision Medical Products, Inc. | 2011-04-08 | 80 | 0 |
| K102862 | NEUROVISION SE (NERVEANA) | Neurovision Medical Products, Inc. | 2010-12-21 | 82 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda