510(k) K912692

CONFORMING BANDAGE by Ulti-Med Intl., Inc. — Product Code NAB

K912692 is an FDA 510(k) premarket notification submitted by Ulti-Med Intl., Inc. for the device "CONFORMING BANDAGE". The FDA issued a decision of Substantially Equivalent on October 4, 1991. The device falls under product code NAB (Gauze / Sponge,Nonresorbable For External Use), a Class I device regulated under 21 CFR 878.4014. Ulti-Med Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 4, 1991
Date Received
June 18, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauze / Sponge,Nonresorbable For External Use
Device Class
Class I
Regulation Number
878.4014
Review Panel
SU
Submission Type