510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K992607Substantially Equivalent

Sonicaid System 8002

Oxford Instruments Medical Systems, Crofton MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992607 is the FDA 510(k) clearance record for SONICAID SYSTEM 8002, a class II device, cleared for Oxford Instruments Medical Systems on under FDA product code HGM (System, Monitoring, Perinatal). FDA records list 5 510(k) clearances for Oxford Instruments Medical Systems, from to . As of , FDA records show no recalls naming K992607.

Clearance record

Decision date
Received
(633 days to decision)
Product code
HGM System, Monitoring, Perinatal
Regulation
21 CFR 884.2740
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Oxford Instruments Medical Systems P.O. Box 4341, Crofton MD
510(k) summary
Summary
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