Atlas FDA

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

Central Medicare Sdn Bhd · Predicate Candidate Screening

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

171 daysmedian FDA review time
240 days90th percentile
15clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K230681Blue Non Sterile Powder Free Nitrile Examination Gloves TestCentral Medicare Sdn Bhd2023-10-022030
K223752Black Non Sterile Powder Free Nitrile Examination Gloves, TeCentral Medicare Sdn Bhd2023-07-242210
K230875Blue Non Sterile Powder Free Nitrile Examination Gloves TestCentral Medicare Sdn Bhd2023-07-201120
K230564Green Non Sterile Powder Free Nitrile Examination GlovesCentral Medicare Sdn Bhd2023-05-23830
K213437Blue Non Sterile Powder Free Nitrile Examination Gloves TestCentral Medicare Sdn Bhd2022-04-111710
K211022Blue Non Sterile Powder Free Nitrile Examination Gloves, TesCentral Medicare Sdn Bhd2021-12-222610
K203036Non Sterile Powder Free Polyurethane Examination Gloves (BluCentral Medicare Sdn Bhd2021-05-072140
K183149Blue Non-Sterile Powder Free Nitrile Examination Gloves, TesCentral Medicare Sdn Bhd2019-07-042330
K173942Blue Non Sterile powder free Nitrile Examination Gloves TestCentral Medicare Sdn Bhd2018-03-05690
K172642Orange Non Sterile Powder Free Nitrile Examination GlovesCentral Medicare Sdn Bhd2017-11-28880
K172525Blue Non Sterile Powder Free Nitrile Examination Gloves TestCentral Medicare Sdn Bhd2017-11-13840
K143247Powder Free Nitrile Examination Gloves, Nonsterile,(Blue,BlaCentral Medicare Sdn Bhd2015-01-22710
K113440HIGH FIVECentral Medicare Sdn Bhd2012-05-231840
K103734POWDER FREE NITRILE EXAMINATION GLOVES WHITE COLORED NON-STECentral Medicare Sdn Bhd2011-08-192400
K093696SR GLOVE, NU GLOVE, HIGHSTRESS MODEL 801, MODEL 802, MODEL 8Central Medicare Sdn Bhd2010-02-12740

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