510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K893981Substantially Equivalent

Watchchild

Monox, Inc., Los Alamitos CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893981 is the FDA 510(k) clearance record for WATCHCHILD, a class II device, cleared for Monox, Inc. on under FDA product code HGM (System, Monitoring, Perinatal). FDA records list one 510(k) clearance for Monox, Inc. As of , FDA records show no recalls naming K893981.

Clearance record

Decision date
Received
(322 days to decision)
Product code
HGM System, Monitoring, Perinatal
Regulation
21 CFR 884.2740
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Monox, Inc. 10572 Calle Lee, Los Alamitos CA
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