510(k) K924542

NASAL-SINUS PACKING by Ultracell Medical Technologies, Inc. — Product Code EMX

K924542 is an FDA 510(k) premarket notification submitted by Ultracell Medical Technologies, Inc. for the device "NASAL-SINUS PACKING". The FDA issued a decision of Substantially Equivalent on February 12, 1993. The device falls under product code EMX (Balloon, Epistaxis), a Class I device regulated under 21 CFR 874.4100. Ultracell Medical Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 12, 1993
Date Received
September 8, 1992
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