510(k) K871917

FRASTEC DRY GAUZE BANDAGE by Fraass Survival Systems, Inc. — Product Code EFQ

K871917 is an FDA 510(k) premarket notification submitted by Fraass Survival Systems, Inc. for the device "FRASTEC DRY GAUZE BANDAGE". The FDA issued a decision of SN on June 16, 1987. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Fraass Survival Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
June 16, 1987
Date Received
May 18, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauze/Sponge, Internal
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type