510(k) K945138
K945138 is an FDA 510(k) premarket notification submitted by Invivo Research, Inc. for the device "OMEGA 5600 SERIES NON-INVASIVE BLOOD PRESSURE MONITORS". The FDA issued a decision of Substantially Equivalent on November 20, 1995. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Invivo Research, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 20, 1995
- Date Received
- October 20, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Measurement, Blood-Pressure, Non-Invasive
- Device Class
- Class II
- Regulation Number
- 870.1130
- Review Panel
- CV
- Submission Type