510(k) K912816
K912816 is an FDA 510(k) premarket notification submitted by S & W Medico Teknik for the device "PRESS 1 PRESS 2 9220 UPDATING OF THE MODULE". The FDA issued a decision of Substantially Equivalent on April 10, 1992. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. S & W Medico Teknik has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 10, 1992
- Date Received
- June 18, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Computer, Blood-Pressure
- Device Class
- Class II
- Regulation Number
- 870.1110
- Review Panel
- CV
- Submission Type