510(k) K861289
K861289 is an FDA 510(k) premarket notification submitted by Burton Medical Products Corp. for the device "BASIC LIGHT". The FDA issued a decision of Substantially Equivalent on April 18, 1986. The device falls under product code KZF (Device, Medical Examination, Ac Powered), a Class I device regulated under 21 CFR 880.6320. Burton Medical Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 18, 1986
- Date Received
- April 7, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Medical Examination, Ac Powered
- Device Class
- Class I
- Regulation Number
- 880.6320
- Review Panel
- HO
- Submission Type