510(k) K991514
K991514 is an FDA 510(k) premarket notification submitted by Gebauer Co. for the device "GEBAUER'S CHLORIDE FINE NOZZE". The FDA issued a decision of Substantially Equivalent on July 16, 1999. The device falls under product code MLY (Vapocoolant Device), a Class U device. Gebauer Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 16, 1999
- Date Received
- April 30, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Vapocoolant Device
- Device Class
- Class U
- Regulation Number
- Review Panel
- PM
- Submission Type