Adler Instrument Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Adler Instrument Co. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Adler Instrument Co. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1983 to 1991.
Browse the FDA 510(k) cleared devices submitted by Adler Instrument Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Adler Instrument Co.
8 devices
Cleared
Feb 01, 1991
MAXI-FLOW SUCTION SET 12 FT.
General Hospital
17d
Cleared
Feb 01, 1991
MAXI-FLOW SUCTION SET W/Y CONNECTOR
General Hospital
17d
Cleared
Dec 21, 1990
MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER
Obstetrics & Gynecology
154d
Cleared
Dec 17, 1990
MAXI-FLOW INSUFFLATOR TUBING SET
Obstetrics & Gynecology
150d
Cleared
Apr 04, 1990
ADLER DISPOSABLE BIPOLAR CORD
Ophthalmic
36d
Cleared
Aug 01, 1984
ADLER CUSTOM PROCEDURE PACKS
General & Plastic Surgery
98d
Cleared
Nov 03, 1983
ADLER STEAM INDICATOR-GAS INDICATOR
General Hospital
44d
Cleared
May 09, 1983
CONTAINER SYSTEM
General & Plastic Surgery
35d