510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834399Substantially Equivalent

New Mother's Way-Breast Pump

Huntleigh Technology, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834399 is the FDA 510(k) clearance record for NEW MOTHER'S WAY-BREAST PUMP, a class I device, cleared for Huntleigh Technology, Inc. on under FDA product code HGY (Pump, Breast, Non-Powered). FDA records list 23 510(k) clearances for Huntleigh Technology, Inc., from to . As of , FDA records show no recalls naming K834399.

Clearance record

Decision date
Received
(34 days to decision)
Product code
HGY Pump, Breast, Non-Powered
Regulation
21 CFR 884.5150
Device class
Class I
Review panel
Obstetrics/Gynecology
Applicant
Huntleigh Technology, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HGY

Trailing 12 months

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

FDA records show no clearances under product code HGY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HGY, 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