Respirizer Co., Div. Campillary Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Respirizer Co., Div. Campillary Systems, Inc. - FDA 510(k) Cleared De...
1
Total
1
Cleared
0
Denied
Respirizer Co., Div. Campillary Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1981 to 1981. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Respirizer Co., Div. Campillary Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Respirizer Co., Div. Campillary Systems, Inc.
1 devices