Absolute Quality Leadership, Inc. is one of 7118 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Absolute Quality Leadership, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POWDER-FREE LATEX EXAMINATION GLOVE, TEAL OR WHITE (NON-COLORED)
1
Total
1
Cleared
0
Denied
Absolute Quality Leadership, Inc. has 1 FDA 510(k) cleared medical devices. Based in Santa Maria, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Absolute Quality Leadership, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Absolute Quality Leadership, Inc.
1 devices