Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Techno-Path Manufacturing , Ltd. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
89 daysmedian FDA review time
496 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K242492 | Multichem ID-G (09339892190); Multichem ID-G (SR102G); Multi | Techno-Path Manufacturing , Ltd. | 2025-12-30 | 496 | 0 |
| K132751 | MULTICHEM S PLUS / S PLUS (ASSAYED) | Techno-Path Manufacturing , Ltd. | 2013-10-22 | 49 | 0 |
| K131993 | MULTICHEM U | Techno-Path Manufacturing , Ltd. | 2013-10-15 | 109 | 0 |
| K131992 | MULTICHEM P | Techno-Path Manufacturing , Ltd. | 2013-09-25 | 89 | 0 |
| K132174 | MULTICHEM WBT | Techno-Path Manufacturing , Ltd. | 2013-09-20 | 67 | 0 |
| K132091 | MULTICHEM IA AND IA PLUS | Techno-Path Manufacturing , Ltd. | 2013-09-20 | 74 | 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