510(k) K863359

BOUFFANT-STYLE SURGICAL CAP by Kimberly-Clark Corp. — Product Code FYF

K863359 is an FDA 510(k) premarket notification submitted by Kimberly-Clark Corp. for the device "BOUFFANT-STYLE SURGICAL CAP". The FDA issued a decision of Substantially Equivalent on September 29, 1986. The device falls under product code FYF (Cap, Surgical), a Class I device regulated under 21 CFR 878.4040. Kimberly-Clark Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 29, 1986
Date Received
September 2, 1986
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