Sandare Chemical Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sandare Chemical Co., Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Sandare Chemical Co., Inc. has 23 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 23 cleared submissions from 1979 to 1987. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Sandare Chemical Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sandare Chemical Co., Inc.
23 devices
Cleared
Sep 29, 1987
EAGLE DIAGNOSTICS GLYCOHEMOGLOBIN UNITIZED TEST
Hematology
71d
Cleared
Aug 08, 1986
SANDARE GLYCOHEMOGLOBIN PROCEDURE
Hematology
36d
Cleared
Mar 17, 1986
SANDARE BCG ALBUMIN PROCEDURE
Chemistry
20d
Cleared
May 07, 1985
SANDARE IRON-BINDING CAPACITY PROCEDURE
Chemistry
28d
Cleared
Apr 30, 1985
SANDARE IRON PROCEDURE
Chemistry
21d
Cleared
Dec 10, 1984
SANDARE ALKALINE PHOSPHATASE PROCEDURE
Chemistry
20d
Cleared
Aug 17, 1984
SANDARE ACID PHOSPHATASE PROCEDURE
Chemistry
38d
Cleared
Jan 13, 1984
TRI-LEVEL BILIRUBIN CONTROLS
Chemistry
60d
Cleared
Nov 07, 1983
TOTAL & DIRECT BILIRUBIN PROCEDURES
Chemistry
69d
Cleared
Sep 12, 1983
ALBUMIN PROCEDURE BCP
Chemistry
39d
Cleared
Aug 24, 1983
SANDARE CALCIUM PROCEDURE
Chemistry
49d
Cleared
Aug 16, 1983
TOTAL PROTEIN PROCEDURE
Chemistry
41d