510(k) K122237
K122237 is an FDA 510(k) premarket notification submitted by Biophotas, Inc. for the device "BIOPHOTAS LIFELIGHT". The FDA issued a decision of Substantially Equivalent on January 3, 2013. The device falls under product code ILY (Lamp, Infrared, Therapeutic Heating), a Class II device regulated under 21 CFR 890.5500. Biophotas, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 2013
- Date Received
- July 26, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lamp, Infrared, Therapeutic Heating
- Device Class
- Class II
- Regulation Number
- 890.5500
- Review Panel
- PM
- Submission Type