510(k) K953879

SURGEON'S CAP by American Threshold Industries, Inc. — Product Code FYF

K953879 is an FDA 510(k) premarket notification submitted by American Threshold Industries, Inc. for the device "SURGEON'S CAP". The FDA issued a decision of Substantially Equivalent on January 5, 1996. The device falls under product code FYF (Cap, Surgical), a Class I device regulated under 21 CFR 878.4040. American Threshold Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 5, 1996
Date Received
August 16, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cap, Surgical
Device Class
Class I
Regulation Number
878.4040
Review Panel
SU
Submission Type