510(k) K940165
K940165 is an FDA 510(k) premarket notification submitted by Unitek Corp. for the device "ALASTIK". The FDA issued a decision of Substantially Equivalent on March 7, 1994. The device falls under product code ECI (Band, Elastic, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Unitek Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 7, 1994
- Date Received
- January 6, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Band, Elastic, Orthodontic
- Device Class
- Class I
- Regulation Number
- 872.5410
- Review Panel
- DE
- Submission Type