Medical Engineering Corp. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Medical Engineering Corp. has 28 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 28 cleared submissions from 1977 to 1993. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medical Engineering Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Engineering Corp.
28 devices
Cleared
Nov 18, 1993
STAND ALONE CYSTOMETROGRAM
Gastroenterology & Urology
85d
Cleared
Mar 13, 1991
SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT
Gastroenterology & Urology
107d
Cleared
Jan 14, 1991
SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDER
General & Plastic Surgery
167d
Cleared
Jul 16, 1990
SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SET
Gastroenterology & Urology
21d
Cleared
Aug 10, 1989
SURGITEK FLAT T-SPAN
General & Plastic Surgery
269d
Cleared
Feb 08, 1989
SURGITEK (R) UROFLOW SYSTEM
Gastroenterology & Urology
189d
Cleared
Aug 11, 1988
SURGITEK CO2 DELIVERY SYSTEM
Gastroenterology & Urology
111d
Cleared
May 26, 1988
SURGITEK FLEXIBLE URETEROSCOPE SU-7 & SU-9
Gastroenterology & Urology
87d
Cleared
May 26, 1988
SURGITEK ARTICULATING URETEROSCOPE MODEL SU-11
Gastroenterology & Urology
87d
Cleared
Sep 26, 1984
SURGITEK RECONSTRUC-NIPPLE PROSTHESIS
General & Plastic Surgery
75d
Cleared
Oct 20, 1983
SURGIKEK PENILE PROSTHESIS TAIL EXTEND
Gastroenterology & Urology
118d
Cleared
Oct 19, 1983
PERCUTANEOUS NEPHROSTOMY CATHETER
Gastroenterology & Urology
43d