Hycel, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hycel, Inc. - FDA 510(k) Cleared Devices
22
Total
21
Cleared
0
Denied
Hycel, Inc. has 21 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1976 to 1980.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hycel, Inc.
22 devices
Cleared
Oct 06, 1980
HYCEL TRIGYCERIDE II TEST
Chemistry
Cleared
Feb 27, 1979
HYCEL M
Chemistry
6d
Cleared
Jan 26, 1979
KETOSTEROID TEST, HYCEL-17
Chemistry
30d
Cleared
Jan 26, 1979
HYCEL LDH-INT TEST
Chemistry
29d
Cleared
Jan 03, 1979
HYCEL COUNTER 333
Hematology
16d
Cleared
Jan 03, 1979
HYCEL COUNTER 222
Hematology
16d
Cleared
Jan 03, 1979
HYCEL COUNTER 211
Hematology
16d
Cleared
Jul 27, 1978
ROYCO MODEL 970 HEMATOLOGY DATA ANALYZER
Hematology
48d
Cleared
Jul 27, 1978
HMA URIC ACID TEST
Chemistry
41d
Cleared
May 03, 1978
LELECTIVE KINETIC SYSTEM-60
Chemistry
42d
Cleared
Apr 05, 1978
DIRECT UREA NITROGEN TEST
Chemistry
47d
Cleared
Jan 30, 1978
17-HYDROXY TEST
Chemistry
34d