Synermed, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Synermed, Inc. - FDA 510(k) Cleared Devices
45
Total
45
Cleared
0
Denied
Synermed, Inc. has 45 FDA 510(k) cleared chemistry devices. Based in Quebec, Canada, CA.
Historical record: 45 cleared submissions from 1990 to 1997.
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 - Synermed, Inc.
45 devices
Cleared
Sep 25, 1997
SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KIT
Chemistry
37d
Cleared
Aug 07, 1997
SYNERMED TOTAL BILIRUBIN REAGENT KIT
Chemistry
17d
Cleared
Jun 26, 1997
SYNERMED IR 200 CHEMISTRY ANALYZER
Chemistry
63d
Cleared
Mar 03, 1997
SYNERMED ISE REAGENTS
Chemistry
250d
Cleared
Dec 18, 1996
SYNERMED DIRECT BILIRUBIN REAGENT KIT
Chemistry
78d
Cleared
Mar 11, 1996
SYNERMED ENZYMATIC CO2 REAGENT KIT
Chemistry
13d
Cleared
Aug 31, 1995
SYNERMED CALCIUM REAGENT KIT
Chemistry
44d
Cleared
Jun 20, 1995
SYNERMED ISE REAGENTS
Chemistry
42d
Cleared
Sep 20, 1994
CREATININE-PO REAGENT KIT
Chemistry
39d
Cleared
May 03, 1994
SYNERMED AMYLASE REAGENT KIT
Chemistry
56d
Cleared
Apr 26, 1994
SYNERMED IR 500 CHEMISTRY ANALYZER
Chemistry
151d
Cleared
Apr 26, 1994
SYNERMED ISE REAGENTS
Chemistry
35d
Looking for a specific device from Synermed, Inc.? Search by device name or K-number.
Search all Synermed, Inc. devices