Hyland Therapeutic Div., Travenol Laboratories - FDA 510(k) Cleared D...
44
Total
44
Cleared
0
Denied
Hyland Therapeutic Div., Travenol Laboratories has 44 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 44 cleared submissions from 1976 to 1982. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Hyland Therapeutic Div., Travenol Laboratories Filter by specialty or product code using the sidebar.
44 devices
Cleared
Apr 26, 1982
ALUMINA SILICA-ACTIVATED PARTIAL THROM
Hematology
31d
Cleared
Mar 11, 1982
HAEMOPHILUS INFLUENZAE TYPE B ANTISERUM
Microbiology
45d
Cleared
Aug 18, 1981
NEPHELOMETRIC SOLID TURBIDITY STANDARD
Immunology
12d
Cleared
Feb 02, 1981
Q-PAK THERAPEUTIC DRUG MONIT. CONTROL S
Chemistry
20d
Cleared
Jan 28, 1981
OMEGA THERAPEUTIC DRUG MONIT. CONTROL S.
Chemistry
15d
Cleared
Jan 05, 1981
ALERT A,HDL-APOLIPOROTEIN A, TEST KIT
Immunology
76d
Cleared
Jun 28, 1979
LOW IONIC STRENGTH SOLUTION (LISS)
Hematology
13d
Cleared
May 16, 1979
TEST CELLS
Hematology
97d
Cleared
Aug 31, 1978
GLOBULIN TEST, HUMAN THYROXINE BINDING
Chemistry
44d
Cleared
Jul 27, 1978
AUTOMATED ENZYME
Hematology
45d
Cleared
Jun 14, 1978
DILUTOR TRANSPORTER
Chemistry
33d
Cleared
Jun 06, 1978
LAS-R HUMAN IGE TEST
Immunology
29d
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