Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
San Diego Biotech · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K980205 | SAN DIEGO BIOTECH HCG PREGNANCY DIPSTICK TEST | San Diego Biotech | 1998-02-12 | 23 | 0 |
| K974851 | SAN DIEGO BIOTECH HCG PREGNANCY URINE TEST | San Diego Biotech | 1998-01-22 | 24 | 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