Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Behn Meyer & Co. (M) Sdn Bhd · 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) |
|---|---|---|---|---|---|
| K892030 | PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES) | Behn Meyer & Co. (M) Sdn Bhd | 1989-05-01 | 31 | 0 |
| K891181 | PATIENT EXAMINATION GLOVES (LATEX) | Behn Meyer & Co. (M) Sdn Bhd | 1989-03-23 | 17 | 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