510(k) K954491

HYDROCELL NASAL AND SINUS PACKS by Smith & Nephew Richards, Inc. — Product Code EMX

K954491 is an FDA 510(k) premarket notification submitted by Smith & Nephew Richards, Inc. for the device "HYDROCELL NASAL AND SINUS PACKS". The FDA issued a decision of Substantially Equivalent on November 15, 1995. The device falls under product code EMX (Balloon, Epistaxis), a Class I device regulated under 21 CFR 874.4100. Smith & Nephew Richards, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 15, 1995
Date Received
September 27, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Balloon, Epistaxis
Device Class
Class I
Regulation Number
874.4100
Review Panel
EN
Submission Type