Sj Medical Products (M) Sdn Bhd: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Sj Medical Products (M) Sdn Bhd” (first 1994, latest 1997), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 52 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
LYYLatex Patient Examination Glove33
LZAPolymer Patient Examination Glove22

Review panels

Most recent Sj Medical Products (M) Sdn Bhd 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K971666SMART - FIT, PREPOWDERED NITRILE EXAMINATION GLOVESLZA1997-07-0358
K971665SMART - FIT, POWDERFREE NITRILE EXAMINATION GLOVESLZA1997-06-2752
K971403SMART - GLOVE POWDER FREE LATEX EXAMINATION GLOVELYY1997-05-2944
K941754POWDER FREE LATEX EXMINATION GLOVESLYY1994-05-0931
K932332PATIENT EXAMINATION GLOVE - POWDEREDLYY1994-03-15306

Recalls

openFDA lists no recalls under a recalling firm named Sj Medical Products (M) Sdn Bhd.

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Sj Medical Products (M) Sdn Bhd?

FDA lists 5 510(k) clearances under the applicant name “Sj Medical Products (M) Sdn Bhd” (first 1994, latest 1997), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Sj Medical Products (M) Sdn Bhd?

The median time from FDA receipt to decision across 510(k)s cleared under the name Sj Medical Products (M) Sdn Bhd is 52 days.

Which FDA product codes appear under Sj Medical Products (M) Sdn Bhd?

The most frequent FDA product codes under this applicant name are LYY (Latex Patient Examination Glove, 3); LZA (Polymer Patient Examination Glove, 2).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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