Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Todd Medical, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
196 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K873288 | CLOSED FOLEY CATHETER SYSTEM | Todd Medical, Inc. | 1987-11-27 | 102 | 0 |
| K873499 | TODD MEDICAL/SKILLED CARE PRODUCTS | Todd Medical, Inc. | 1987-11-24 | 85 | 0 |
| K873287 | IRRIGATION TRAY (W/120CC OF STERILE NORMAL SALINE) | Todd Medical, Inc. | 1987-11-13 | 88 | 0 |
| K873469 | TODD MEDICAL/SKILLED CARE PRODUCTS | Todd Medical, Inc. | 1987-10-29 | 62 | 0 |
| K850646 | ECLIPSE SELF ADHERING ELECTRODE | Todd Medical, Inc. | 1985-09-03 | 196 | 0 |
| K850004 | TRANSCUTANEOUS NERVE STIMULATOR FOR PAIN RELIEF | Todd Medical, Inc. | 1985-04-02 | 90 | 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