510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771981Substantially Equivalent

Minimap Model 810

Applied Medical Research, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771981 is the FDA 510(k) clearance record for MINIMAP MODEL 810, a class II device, cleared for Applied Medical Research on under FDA product code DSK (Computer, Blood-Pressure). FDA records list 22 510(k) clearances for Applied Medical Research, from to . As of , FDA records show no recalls naming K771981.

Clearance record

Decision date
Received
(98 days to decision)
Product code
DSK Computer, Blood-Pressure
Regulation
21 CFR 870.1110
Device class
Class II
Review panel
Cardiovascular
Applicant
Applied Medical Research 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DSK

Trailing 12 months

FDA records hold no clearances under product code DSK in the trailing twelve months.

FDA records show no clearances under product code DSK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DSK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260