Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Electrophoresis Corp. — 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) |
|---|---|---|---|---|---|
| K802395 | SPECIAL PROCEDURE AQAROSE FILM | Electrophoresis Corp. | 1980-11-26 | 55 | 0 |
| K790309 | CPK ISOENZYME SUBSTRATE | Electrophoresis Corp. | 1979-04-04 | 50 | 0 |
| K790310 | HEMOGLOBIN CONTROLS | Electrophoresis Corp. | 1979-03-21 | 36 | 0 |
| K790311 | LDH ISOENZYME REAGENT | Electrophoresis Corp. | 1979-03-21 | 36 | 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