Zimmar Consulting , Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Zimmar Consulting , Ltd. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 17 cleared submissions from 1984 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Zimmar Consulting , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zimmar Consulting , Ltd.
17 devices
Cleared
Apr 07, 1986
CLINISET INFUSION SET
General Hospital
68d
Cleared
Dec 05, 1984
PHARMA-PLAST RECTAL TIP
Gastroenterology & Urology
90d
Cleared
Dec 05, 1984
PHARMA-PLAST URIDROP-URIDOME
Gastroenterology & Urology
90d
Cleared
Nov 23, 1984
PHARMA-PLAST SUCTION SET TYPE YANKAUER
General & Plastic Surgery
78d
Cleared
Nov 19, 1984
PHARMA-PLAST OXYGEN CATHETER
Anesthesiology
74d
Cleared
Nov 19, 1984
PHARMA-PLAST NASAL OXYGEN CANNULA
Anesthesiology
74d
Cleared
Nov 19, 1984
PHARMA-PLAST SUCTION TIP, TYPE ORTHOPAE-
General Hospital
74d
Cleared
Nov 16, 1984
PHARMA-PLAST CONNECTING TUBE TYPE SUCT-
General Hospital
71d
Cleared
Oct 31, 1984
PHARMA-PLAST SYRINGE
General Hospital
55d
Cleared
Oct 31, 1984
PHARMA-PLAST SYRINGE WITH NEEDLE
General Hospital
55d
Cleared
Oct 31, 1984
PHARMA-PLAST INSULIN SYRINGE
General Hospital
55d
Cleared
Oct 31, 1984
PHARMA-PLAST SINGLE USE OVERSHOES
General Hospital
55d