510(k) K962605

PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE) by Surgicot, Inc. — Product Code FRG

K962605 is an FDA 510(k) premarket notification submitted by Surgicot, Inc. for the device "PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE)". The FDA issued a decision of Substantially Equivalent on March 11, 1997. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. Surgicot, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 1997
Date Received
July 2, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wrap, Sterilization
Device Class
Class II
Regulation Number
880.6850
Review Panel
HO
Submission Type