510(k) K771981
K771981 is an FDA 510(k) premarket notification submitted by Applied Medical Research for the device "MINIMAP MODEL 810". The FDA issued a decision of Substantially Equivalent on January 24, 1978. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. Applied Medical Research has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 24, 1978
- Date Received
- October 18, 1977
- 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