510(k) K901957
K901957 is an FDA 510(k) premarket notification submitted by Lancer Orthodontics, Inc. for the device "MUSTANG, C.A.T.". The FDA issued a decision of Substantially Equivalent on July 30, 1990. The device falls under product code EJF (Bracket, Metal, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Lancer Orthodontics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 30, 1990
- Date Received
- May 1, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bracket, Metal, Orthodontic
- Device Class
- Class I
- Regulation Number
- 872.5410
- Review Panel
- DE
- Submission Type