510(k) K110001
K110001 is an FDA 510(k) premarket notification submitted by Spacelabs Healthcare, Ltd. for the device "SPACELABS PATHFINDER SL HOLTER ANALYZER". The FDA issued a decision of Substantially Equivalent on June 14, 2011. The device falls under product code DQK (Computer, Diagnostic, Programmable), a Class II device regulated under 21 CFR 870.1425. Spacelabs Healthcare, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 14, 2011
- Date Received
- January 3, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Computer, Diagnostic, Programmable
- Device Class
- Class II
- Regulation Number
- 870.1425
- Review Panel
- CV
- Submission Type