510(k) K950854
K950854 is an FDA 510(k) premarket notification submitted by Vitalograph , Ltd. for the device "VITALOGRAPH 2110 SOFTWARE INTERFACE". The FDA issued a decision of Substantially Equivalent on October 12, 1995. The device falls under product code DSH (Recorder, Magnetic Tape, Medical), a Class II device regulated under 21 CFR 870.2800. Vitalograph , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 12, 1995
- Date Received
- February 27, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Recorder, Magnetic Tape, Medical
- Device Class
- Class II
- Regulation Number
- 870.2800
- Review Panel
- CV
- Submission Type