510(k) K012868
K012868 is an FDA 510(k) premarket notification submitted by Micromedics, Inc. for the device "MICROMEDICS FIBRIJET AEROSOL APPLICATOR". The FDA issued a decision of Substantially Equivalent on October 29, 2001. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Micromedics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 29, 2001
- Date Received
- August 27, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Piston
- Device Class
- Class II
- Regulation Number
- 880.5860
- Review Panel
- HO
- Submission Type