Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Cranberry (M) Sdn. Bhd. · Predicate Candidate Screening

4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K984039CRANBERRY POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN Cranberry (M) Sdn. Bhd.1999-03-291370
K983334NITRILE POWDER FREE EXAMINATION GLOVESCranberry (M) Sdn. Bhd.1999-02-191490
K935946POWDER FREE LATEX EXAMINATION GLOVESCranberry (M) Sdn. Bhd.1994-06-211900
K890976PATIENT EXAMINATION GLOVECranberry (M) Sdn. Bhd.1989-04-18500

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