Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Northwest Medical Physics Equipment, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
210 daysmedian FDA review time
343 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K063274 | ACCULOC BREAST LOCALIZATION SYSTEM | Northwest Medical Physics Equipment, Inc. | 2006-12-12 | 43 | 0 |
| K012575 | PREFERNCE IMRT TREATMENT PLANNING MODULE | Northwest Medical Physics Equipment, Inc. | 2002-03-12 | 215 | 0 |
| K001833 | PREFERENCE TREATMENT SYSTEM | Northwest Medical Physics Equipment, Inc. | 2000-09-28 | 104 | 0 |
| K983793 | PREFERENCE TREATMENT SYSTEM | Northwest Medical Physics Equipment, Inc. | 1999-10-05 | 343 | 0 |
| K970464 | P REFERENCE TPS (TREATMENT PLANNING SOFTWARE) 1.1 | Northwest Medical Physics Equipment, Inc. | 1997-09-05 | 210 | 0 |
| K960293 | MRTOFLM COMPUTER PROGRAM | Northwest Medical Physics Equipment, Inc. | 1996-08-01 | 198 | 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