Packard Instrument Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Packard Instrument Co., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Packard Instrument Co., Inc. has 4 FDA 510(k) cleared medical devices. Based in Downers Grove, US.
Historical record: 4 cleared submissions from 1988 to 1992. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Packard Instrument Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Packard Instrument Co., Inc.
4 devices