510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902690Substantially Equivalent

Sonicaid Model Meridian 800

Oxford Medilog, Inc., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902690 is the FDA 510(k) clearance record for SONICAID MODEL MERIDIAN 800, a class II device, cleared for Oxford Medilog, Inc. on under FDA product code HGM (System, Monitoring, Perinatal). FDA records list 48 510(k) clearances for Oxford Medilog, Inc., from to . As of , FDA records show no recalls naming K902690.

Clearance record

Decision date
Received
(231 days to decision)
Product code
HGM System, Monitoring, Perinatal
Regulation
21 CFR 884.2740
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Oxford Medilog, Inc. 11526 53rd. St. N., Clearwater FL
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