Surgicot, Inc.
Surgicot, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1997.
Top product codes for Surgicot, Inc.
Recent clearances by Surgicot, Inc.
- K962605 — PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE)
- K931270 — SURGICLEAN ENZYMATIC INSTRUMENT CLEANER
- K863122 — ASSERT BIOLOGICAL/CHEMICAL INDICATOR 12 MONTH EXP.
- K855101 — ASSERT TM BIOLOGICAL/CHEMICAL INDICATOR
- K854631 — ASSERT EO BIOLOGICAL TEST PACK
- K854902 — SURGICOT STEAM TEST PACK
- K840541 — NEURO SPONGE
- K840471 — EYE SPEAR
- K840470 — SURGISCRIBE MARKING PEN
- K830739 — PRO-GUARD
- K820302 — SURGIPEEL SELF-SEAL PACKAGING SYSTEM
- K800029 — SURGICOT 2 INDICATOR SYSTEM
- K771846 — SUOGIPEEL PACKAGING SYSTEM
- K771032 — POUCHES, PEEL OPEN, BREATHABLE
- K770593 — CORRUGATED TUBING #770 & 771
- K770585 — AEROSOL T ADAPTER, #752
- K770586 — UNIVERSAL MOUTHPIECE, #750
- K770587 — VENTILATOR ADAPTOR, #751
- K761254 — BAND-AGE ICE-BANDAGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.