510(k) K771981

MINIMAP MODEL 810 by Applied Medical Research — Product Code DSK

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