Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Precision Med Products, Ltd. — Predicate Candidate Screening
16 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
50 daysmedian FDA review time
59 days90th percentile
16clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K932711 | PRECISION MED PRODUCTS LTD GUEDEL AIRWAYS | Precision Med Products, Ltd. | 1993-07-23 | 49 | 0 |
| K932708 | PRECISION MED PRODUCTS LTD MAPLESON D CIRCUITS | Precision Med Products, Ltd. | 1993-07-23 | 49 | 0 |
| K932706 | PRECISION MED PRODUCTS LTD. VENTILATOR HOSE | Precision Med Products, Ltd. | 1993-07-23 | 49 | 0 |
| K932710 | GAS SAMPLING LINES AND CONNECTORS | Precision Med Products, Ltd. | 1993-07-23 | 49 | 0 |
| K932707 | ADULT ANESTHESIA BREATHING CIRCUIT | Precision Med Products, Ltd. | 1993-07-23 | 49 | 0 |
| K932709 | PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM | Precision Med Products, Ltd. | 1993-07-23 | 49 | 0 |
| K932712 | PRECISION MED PRODUCTS LTD VOLUME VENTILATORS | Precision Med Products, Ltd. | 1993-07-22 | 48 | 0 |
| K932497 | PRECISION MED PRODUCTS, LTD. ADULT GAS SAMPLING | Precision Med Products, Ltd. | 1993-07-22 | 59 | 0 |
| K932489 | PMP, LTD. ADULT TEMP. MONITORING ANESTHESIA CIR. | Precision Med Products, Ltd. | 1993-07-22 | 59 | 0 |
| K932488 | PMP, LTD. PEDIATRIC GAS SAMPLING CIRCUITS | Precision Med Products, Ltd. | 1993-07-22 | 59 | 0 |
| K932486 | PMP, LTD. PEDIATRIC TEMPERATURE MONITORING CIRCUIT | Precision Med Products, Ltd. | 1993-07-21 | 58 | 0 |
| K932496 | PRECISION MED PRODUCTS, LTD. BREATHING BAGS | Precision Med Products, Ltd. | 1993-07-16 | 52 | 0 |
| K932490 | PMP, LTD. CUSTOM ANESTHESIA CIRCUITS | Precision Med Products, Ltd. | 1993-07-14 | 51 | 0 |
| K932487 | PMP, LTD. PEDIATRIC ANESTHESIA CIRCUITS | Precision Med Products, Ltd. | 1993-07-13 | 50 | 0 |
| K932485 | PRECISION MED PRODUCTS, LTD. COAXIAL CIRCUITS | Precision Med Products, Ltd. | 1993-07-13 | 50 | 0 |
| K931345 | CONNECTORS AND AIRWAY EXTENSIONS | Precision Med Products, Ltd. | 1993-04-23 | 37 | 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