510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071800Substantially Equivalent

Philips Avalon Fetal Monitors Fm20 and Fm30

Philips Medizinsysteme Boeblingen GmbH, Cardiac an, Boeblingen, Baden-Wuerttemberg, DE / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071800 is the FDA 510(k) clearance record for PHILIPS AVALON FETAL MONITORS FM20 AND FM30, a class II device, cleared for Philips Medizinsysteme Boeblingen GmbH, Cardiac AN on under FDA product code HGM (System, Monitoring, Perinatal). FDA records list 25 510(k) clearances for Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, from to . As of , FDA records show 4 recalls naming K071800.

Clearance record

Decision date
Received
(87 days to decision)
Product code
HGM System, Monitoring, Perinatal
Regulation
21 CFR 884.2740
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Philips Medizinsysteme Boeblingen GmbH, Cardiac AN Hewlett-Packard St. 2, Boeblingen, Baden-Wuerttemberg, DE
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