Sanrea Healthcare Private Limited is one of 128 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Sanrea Healthcare Private Limited - FDA 510(k) Cleared Devices
Recent clearances: STERILE PATIENT POWDERFREE LATEX EXAMINATION GLOVES, POWDER FREE LATEX SURGEON'S GLOVES CONTAINS 50 MEGM OR LESS OF TOTAL WATER EXTRACTABLE PER GRAM, STERILE POWDERED LATEX PATIENT EXAMINATION GLOVES
4
Total
4
Cleared
0
Denied
Sanrea Healthcare Private Limited has 4 FDA 510(k) cleared medical devices. Based in Kerala, IN.
Historical record: 4 cleared submissions from 2003 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sanrea Healthcare Private Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sanrea Healthcare Private Limited
4 devices
Cleared
Feb 11, 2003
STERILE PATIENT POWDERFREE LATEX EXAMINATION GLOVES
General Hospital
78d
Cleared
Feb 11, 2003
POWDER FREE LATEX SURGEON'S GLOVES CONTAINS 50 MEGM OR LESS OF TOTAL WATER...
General Hospital
78d
Cleared
Feb 11, 2003
STERILE POWDERED LATEX PATIENT EXAMINATION GLOVES
General Hospital
78d
Cleared
Jan 16, 2003
PRE-POWDERED LATEX SURGEON'S GLOVES
General Hospital
87d