510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K910815Substantially Equivalent

Cr Spiral Electrode

Neward Enterprises, Inc., Cucamonga CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910815 is the FDA 510(k) clearance record for CR SPIRAL ELECTRODE, a class II device, cleared for Neward Enterprises, Inc. on under FDA product code HGP (Electrode, Circular (Spiral), Scalp And Applicator). FDA records list 8 510(k) clearances for Neward Enterprises, Inc., from to . As of , FDA records show no recalls naming K910815.

Clearance record

Decision date
Received
(287 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
Neward Enterprises, Inc. P.O. Box 725, Cucamonga CA
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