510(k) K830739

PRO-GUARD by Surgicot, Inc. — Product Code FRG

K830739 is an FDA 510(k) premarket notification submitted by Surgicot, Inc. for the device "PRO-GUARD". The FDA issued a decision of Substantially Equivalent on March 29, 1983. 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 29, 1983
Date Received
March 8, 1983
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