510(k) K940776
K940776 is an FDA 510(k) premarket notification submitted by Kreativ, Inc. for the device "KREATIV MODEL KV-1". The FDA issued a decision of Substantially Equivalent on December 21, 1994. The device falls under product code KOJ (Airbrush), a Class II device regulated under 21 CFR 872.6080. Kreativ, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 21, 1994
- Date Received
- February 22, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Airbrush
- Device Class
- Class II
- Regulation Number
- 872.6080
- Review Panel
- DE
- Submission Type