510(k) K932913

FERRIS POLYMEM HYDROPHILIC WOUND DRESSING by Ferris Mfg. Corp. — Product Code KMF

K932913 is an FDA 510(k) premarket notification submitted by Ferris Mfg. Corp. for the device "FERRIS POLYMEM HYDROPHILIC WOUND DRESSING". The FDA issued a decision of SN on June 7, 1994. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Ferris Mfg. Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
June 7, 1994
Date Received
June 16, 1993
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