Surgicot, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Surgicot, Inc. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1977 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Surgicot, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgicot, Inc.
19 devices
Cleared
Mar 11, 1997
PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE)
General Hospital
252d
Cleared
Apr 13, 1994
SURGICLEAN ENZYMATIC INSTRUMENT CLEANER
General Hospital
401d
Cleared
Dec 17, 1986
ASSERT BIOLOGICAL/CHEMICAL INDICATOR 12 MONTH EXP.
General Hospital
125d
Cleared
Jul 17, 1986
ASSERT TM BIOLOGICAL/CHEMICAL INDICATOR
General Hospital
206d
Cleared
May 27, 1986
ASSERT EO BIOLOGICAL TEST PACK
General Hospital
190d
Cleared
May 20, 1986
SURGICOT STEAM TEST PACK
General Hospital
162d
Cleared
Apr 23, 1984
NEURO SPONGE
General & Plastic Surgery
75d
Cleared
Mar 16, 1984
EYE SPEAR
Ophthalmic
42d
Cleared
Mar 12, 1984
SURGISCRIBE MARKING PEN
General & Plastic Surgery
38d
Cleared
Mar 29, 1983
PRO-GUARD
General Hospital
21d
Cleared
Feb 24, 1982
SURGIPEEL SELF-SEAL PACKAGING SYSTEM
General Hospital
20d
Cleared
Mar 12, 1980
SURGICOT 2 INDICATOR SYSTEM
General Hospital
65d
Cleared
Oct 13, 1977
SUOGIPEEL PACKAGING SYSTEM
General Hospital
15d
Cleared
Jul 14, 1977
POUCHES, PEEL OPEN, BREATHABLE
General Hospital
35d
Cleared
Apr 19, 1977
CORRUGATED TUBING #770 & 771
Anesthesiology
22d
Cleared
Apr 05, 1977
AEROSOL T ADAPTER, #752
Anesthesiology
8d
Cleared
Apr 05, 1977
UNIVERSAL MOUTHPIECE, #750
Anesthesiology
8d
Cleared
Apr 05, 1977
VENTILATOR ADAPTOR, #751
Anesthesiology
8d
Cleared
Feb 24, 1977
BAND-AGE ICE-BANDAGE
Physical Medicine
73d