510(k) K001624
K001624 is an FDA 510(k) premarket notification submitted by Gebauer Co. for the device "GEBAUER'S FLUORI-METHANE, MODEL 0386-0003-04". The FDA issued a decision of Substantially Equivalent on January 25, 2001. 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
- January 25, 2001
- Date Received
- May 26, 2000
- 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