510(k) K813385
K813385 is an FDA 510(k) premarket notification submitted by Conphar, Inc. for the device "DIGITAL BLOOD PRESSURE UNIT". The FDA issued a decision of Substantially Equivalent on Jan 29, 1982. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Conphar, Inc. has 121 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 29, 1982
- Date Received
- Dec 2, 1981
- 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
- 510(k)