510(k) K950723
K950723 is an FDA 510(k) premarket notification submitted by Biosensor Corp. for the device "AMBULATORY (HOLTER) RECORDING SYSTEM". The FDA issued a decision of Substantially Equivalent on February 9, 1996. The device falls under product code DQK (Computer, Diagnostic, Programmable), a Class II device regulated under 21 CFR 870.1425. Biosensor Corp. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 9, 1996
- Date Received
- February 16, 1995
- 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