510(k) K851055
K851055 is an FDA 510(k) premarket notification submitted by Gac Intl., Inc. for the device "SENTINOL -ORTHODONTIC ARCH WIRE". The FDA issued a decision of Substantially Equivalent on May 9, 1985. The device falls under product code DZC (Wire, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Gac Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 1985
- Date Received
- March 14, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wire, Orthodontic
- Device Class
- Class I
- Regulation Number
- 872.5410
- Review Panel
- DE
- Submission Type