510(k) K895920

VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS by Vitaphore Corp. — Product Code KGX

K895920 is an FDA 510(k) premarket notification submitted by Vitaphore Corp. for the device "VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS". The FDA issued a decision of Substantially Equivalent on June 6, 1991. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Vitaphore Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 1991
Date Received
October 11, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tape And Bandage, Adhesive
Device Class
Class I
Regulation Number
880.5240
Review Panel
SU
Submission Type