510(k) K944468

KERLIX ZINC SALINE DRESSING by Kendall Healthcare Products Co. Div.Of Tyco Health — Product Code KMF

K944468 is an FDA 510(k) premarket notification submitted by Kendall Healthcare Products Co. Div.Of Tyco Health for the device "KERLIX ZINC SALINE DRESSING". The FDA issued a decision of SN on November 29, 1994. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Kendall Healthcare Products Co. Div.Of Tyco Health has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
November 29, 1994
Date Received
September 9, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Liquid
Device Class
Class I
Regulation Number
880.5090
Review Panel
SU
Submission Type