510(k) K950024

EXPANDACELL NASAL PACK WITH AIRWAY by Shippert Medical Technologies Corp. — Product Code EMX

K950024 is an FDA 510(k) premarket notification submitted by Shippert Medical Technologies Corp. for the device "EXPANDACELL NASAL PACK WITH AIRWAY". The FDA issued a decision of Substantially Equivalent on February 17, 1995. The device falls under product code EMX (Balloon, Epistaxis), a Class I device regulated under 21 CFR 874.4100. Shippert Medical Technologies Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 17, 1995
Date Received
January 4, 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