J. Sklar Mfg. Co., Inc. is one of 14456 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
J. Sklar Mfg. Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: JACOBS HIGH VACUUM SUCTION UNIT 05-2570, TISCHLER CERVICAL BIOPSY PUNCH FORCEPS, KOGAN ENDOSPECULUM 9-1/2
18
Total
18
Cleared
0
Denied
J. Sklar Mfg. Co., Inc. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1977 to 1984.
Browse the FDA 510(k) cleared devices submitted by J. Sklar Mfg. Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - J. Sklar Mfg. Co., Inc.
18 devices
Cleared
Oct 31, 1984
JACOBS HIGH VACUUM SUCTION UNIT 05-2570
General & Plastic Surgery
42d
Cleared
Jul 03, 1984
TISCHLER CERVICAL BIOPSY PUNCH FORCEPS
Obstetrics & Gynecology
35d
Cleared
Jun 19, 1984
KOGAN ENDOSPECULUM 9-1/2
General & Plastic Surgery
21d
Cleared
Sep 14, 1982
SCISSORS, VARIOUS
General & Plastic Surgery
29d
Cleared
Jan 12, 1981
KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610
Obstetrics & Gynecology
96d
Cleared
Jan 12, 1981
KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611
Obstetrics & Gynecology
96d
Cleared
Jul 28, 1980
MAGILL CATHETER INTRO. FORCEPS
Gastroenterology & Urology
60d
Cleared
Apr 08, 1980
RUDD-CLINIC HEMORRHOIDAL FORCEPS
Gastroenterology & Urology
40d
Cleared
Apr 23, 1979
HEMORRHOIDAL LIGATOR
General & Plastic Surgery
26d
Cleared
Jan 03, 1978
MINICLAMPS, STABILIZ., FALLOPIAN TUBE
Obstetrics & Gynecology
28d
Cleared
Jan 03, 1978
CANNULA, PERFUSION, FALLOPIAN TUBE
Obstetrics & Gynecology
28d
Cleared
Oct 04, 1977
THOREK SCISSORS 7 1/4 & 10
General & Plastic Surgery
11d