Manan Manufacturing Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Manan Manufacturing Co., Inc. - FDA 510(k) Cleared Devices
20
Total
16
Cleared
0
Denied
Manan Manufacturing Co., Inc. has 16 FDA 510(k) cleared medical devices. Based in Skokie, US.
Historical record: 16 cleared submissions from 1985 to 1987. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Manan Manufacturing Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Manan Manufacturing Co., Inc.
20 devices
Cleared
Aug 25, 1987
MANAN TURNER STYLE NEEDLE
Gastroenterology & Urology
11d
Cleared
Dec 18, 1986
MANAN CONTRAST MEDIA ADMINISTRATION SET
General Hospital
38d
Cleared
Oct 14, 1986
MANAN BREST TUMOR LOCALIZATION NEEDLE
General & Plastic Surgery
14d
Cleared
Jul 11, 1985
NAMAN POTTS COURNAND NEEDLE
Cardiovascular
76d
Cleared
Jul 11, 1985
MANAN SELDINGER NEEDLE
Cardiovascular
76d
Cleared
Jul 11, 1985
MANAN GWI GUIDE WIRE INTRODUCER
Cardiovascular
76d
Cleared
Jul 11, 1985
ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR
General & Plastic Surgery
64d
Cleared
Jul 11, 1985
MYELOGRAM PROCEDURE TRAY
General & Plastic Surgery
29d
Cleared
Jun 27, 1985
MANAN TROCAR STYLE BIOPSY NEEDLE
General & Plastic Surgery
20d
Cleared
Jun 27, 1985
MANAN SPINAL NEEDLE
General & Plastic Surgery
20d
Cleared
Jun 27, 1985
MANAN EPIDURAL NEEDLE
General & Plastic Surgery
20d
Cleared
Jun 21, 1985
MANAN MENGHINI NEEDLE
Gastroenterology & Urology
54d