510(k) K942748

INTRASITE by Smith & Nephew United, Inc. — Product Code NAE

K942748 is an FDA 510(k) premarket notification submitted by Smith & Nephew United, Inc. for the device "INTRASITE". The FDA issued a decision of SN on June 29, 1994. The device falls under product code NAE (Dressing, Wound, Hydrogel Without Drug And/Or Biologic), a Class I device regulated under 21 CFR 878.4022. Smith & Nephew United, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
June 29, 1994
Date Received
June 10, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound, Hydrogel Without Drug And/Or Biologic
Device Class
Class I
Regulation Number
878.4022
Review Panel
SU
Submission Type