510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K822584Substantially Equivalent

Multi-Prong Fetal Scalp Electrode

Kontron Instruments, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822584 is the FDA 510(k) clearance record for MULTI-PRONG FETAL SCALP ELECTRODE, a class II device, cleared for Kontron Instruments, Inc. on under FDA product code HGP (Electrode, Circular (Spiral), Scalp And Applicator). FDA records list 58 510(k) clearances for Kontron Instruments, Inc., from to . As of , FDA records show no recalls naming K822584.

Clearance record

Decision date
Received
(182 days to decision)
Product code
HGP Electrode, Circular (Spiral), Scalp And Applicator
Regulation
21 CFR 884.2675
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Kontron Instruments, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HGP

Trailing 12 months

FDA records hold no clearances under product code HGP in the trailing twelve months.

FDA records show no clearances under product code HGP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HGP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260