Remel Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Remel Co. - FDA 510(k) Cleared Devices
137
Total
137
Cleared
0
Denied
Remel Co. has 137 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 137 cleared submissions from 1979 to 2001.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Remel Co.
137 devices
Cleared
Nov 26, 2001
BACTI-SWAB DRY
Microbiology
19d
Cleared
Jan 22, 1997
A.C.T. I
Microbiology
30d
Cleared
Jan 22, 1997
A.C.T. IV
Microbiology
30d
Cleared
Jan 22, 1997
A.C.T. III
Microbiology
30d
Cleared
Jan 22, 1997
A.C.T. II
Microbiology
30d
Cleared
Mar 19, 1996
CALCOFLUOR WHITE STAIN KIT
Microbiology
68d
Cleared
Mar 19, 1996
BACTIDROP CALCOFLUOR WHITE
Microbiology
68d
Cleared
Feb 23, 1996
REMEL CEFEPIME 30 UG SUSCEPTIBILITY DISK
Microbiology
72d
Cleared
Sep 19, 1994
SYNERGY QUAD
Microbiology
179d
Cleared
Sep 19, 1994
BHI AGAR WITH VANCOMYCIN
Microbiology
179d
Cleared
May 20, 1994
BACTICARD STREP
Microbiology
154d
Cleared
Apr 20, 1994
RIM E.COLI 0157:H7 LATEX TEST
Microbiology
280d
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