Perusahaan Pelindung Getah (M) Sdn Bhd is one of 368 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Perusahaan Pelindung Getah (M) Sdn Bhd - FDA 510(k) Cleared Devices
Recent clearances: POWDER FREE NATURAL RUBBER LOW MODULUS LATEX PATIENT EXAMINATION GLOVES WITH A PROTEIN LABELING CLAIM, RUBBERCARE POWDERED LATEX EXAMINATION GLOVES, RUBBERCARE POLYMER-COATED POWDERED LATEX EXAMINATION GLOVES/GUARDIAN POLYMER-COATED POWDERED EXAMINATION GLOVES. CONTAI
Perusahaan Pelindung Getah (M) Sdn Bhd has 8 FDA 510(k) cleared medical devices. Based in Seremban, N.S., MY.
Historical record: 8 cleared submissions from 1989 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Perusahaan Pelindung Getah (M) Sdn Bhd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.