510(k) K920358
K920358 is an FDA 510(k) premarket notification submitted by Ultracell Medical Technologies, Inc. for the device "ULTRACELL NASAL PACKING". The FDA issued a decision of Substantially Equivalent on November 30, 1992. 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
- November 30, 1992
- Date Received
- January 27, 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