Gibco Laboratories Life Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gibco Laboratories Life Technologies, Inc. - FDA 510(k) Cleared Devic...
67
Total
67
Cleared
0
Denied
Gibco Laboratories Life Technologies, Inc. has 67 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 67 cleared submissions from 1976 to 1987.
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 - Gibco Laboratories Life Technologies, Inc.
67 devices
Cleared
May 26, 1987
SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM
Microbiology
13d
Cleared
Apr 29, 1987
MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226
Microbiology
9d
Cleared
Feb 04, 1987
MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE
Microbiology
22d
Cleared
Jan 05, 1987
PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM
Microbiology
31d
Cleared
Oct 29, 1986
LOMBARD DOWELL AGAR BASE
Microbiology
14d
Cleared
Oct 09, 1986
MUELLER HINTON AGAR W/4%NACL AND OXACILLIN
Microbiology
9d
Cleared
Oct 08, 1986
DRI-FORM: GBNA LISTERIA MEDIUM NO. M22300
Microbiology
8d
Cleared
Sep 03, 1986
CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN
Microbiology
9d
Cleared
Jul 02, 1986
MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM
Microbiology
6d
Cleared
May 20, 1986
SENSITITRE AUTO ID PLATE, AP70
Microbiology
62d
Cleared
May 16, 1986
REGAN-LOWE AGAR
Microbiology
10d
Cleared
May 06, 1986
SENSITITRE SUSCEPTIBILITY PLATES
Microbiology
68d
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