Hayes Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hayes Products, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Hayes Products, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1977 to 1979. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hayes Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hayes Products, Inc.
5 devices
Cleared
Jul 24, 1979
STRESS/EMERGENCY EELCTRODE
Neurology
76d
Cleared
Jul 10, 1979
PREGELLED DISPOSABLE ECG ELECTRODES
Cardiovascular
22d
Cleared
Jul 10, 1979
PREGELLED DISPOSABLE EELCTRO. SERIES 600
Cardiovascular
22d
Cleared
Nov 29, 1978
EKG ELECTRODES, DISPOSABLE
Cardiovascular
9d
Cleared
Aug 04, 1977
PREGELLED DISP. EKG MONITORING ELECT-
Cardiovascular
2d