510(k) K905136

GAUZE SPONGES, INTERNAL AND EXTERNAL by American Healthcare Corp. — Product Code EFQ

K905136 is an FDA 510(k) premarket notification submitted by American Healthcare Corp. for the device "GAUZE SPONGES, INTERNAL AND EXTERNAL". The FDA issued a decision of Substantially Equivalent on March 6, 1991. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. American Healthcare Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 6, 1991
Date Received
November 15, 1990
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