510(k) K955833

NIOMED SURGICAL CAPS by Amerasia Corp. — Product Code FYF

K955833 is an FDA 510(k) premarket notification submitted by Amerasia Corp. for the device "NIOMED SURGICAL CAPS". The FDA issued a decision of Substantially Equivalent on March 15, 1996. The device falls under product code FYF (Cap, Surgical), a Class I device regulated under 21 CFR 878.4040. Amerasia Corp. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 15, 1996
Date Received
December 26, 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