510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K120018Substantially Equivalent

Mindchild Meridian Fetal Heart Rate Monitor

Mindchild Medical, Providence RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120018 is the FDA 510(k) clearance record for MINDCHILD MERIDIAN FETAL HEART RATE MONITOR, a class II device, cleared for Mindchild Medical on under FDA product code HGM (System, Monitoring, Perinatal). FDA records list 3 510(k) clearances for Mindchild Medical, from to . As of , FDA records show no recalls naming K120018.

Clearance record

Decision date
Received
(260 days to decision)
Product code
HGM System, Monitoring, Perinatal
Regulation
21 CFR 884.2740
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Mindchild Medical 755 Westminster St., Providence RI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HGM

Trailing 12 months
2 clearances under product code HGM in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HGM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260