510(k) K943417
K943417 is an FDA 510(k) premarket notification submitted by Jon-Ko Products, Inc. for the device "ORTHODONTIC ELASTOMERIC TUBE/THREAD". The FDA issued a decision of Substantially Equivalent on May 23, 1995. The device falls under product code ECI (Band, Elastic, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Jon-Ko Products, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 23, 1995
- Date Received
- July 15, 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