Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Reed Products, Inc. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K841898 | FIRST RESPONSE EMERG. MEDICSL - BURNS | Reed Products, Inc. | 1984-08-14 | 99 | 0 |
| K841897 | FIRST RESPONSE EMERG. MEDICAL SYSTEM | Reed Products, Inc. | 1984-07-23 | 77 | 0 |
| K841900 | FIRST RESPONSE EMERG. EYE INJURIES | Reed Products, Inc. | 1984-07-23 | 77 | 0 |
| K841899 | FIRST RESPONSE EMERG. MEDICAL SYS BONES | Reed Products, Inc. | 1984-07-23 | 77 | 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