Cleared Traditional

K233880 - Momcozy Wearable Breast Pump (BP137) (FDA 510(k) Clearance)

Also includes:
Momcozy Wearable Breast Pump (BP141)
Mar 2024
Decision
89d
Days
Class 2
Risk

K233880 is an FDA 510(k) clearance for the Momcozy Wearable Breast Pump (BP137). This device is classified as a Pump, Breast, Powered (Class II - Special Controls, product code HGX).

Submitted by Shenzhen Root Innovation Technology Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on March 6, 2024, 89 days after receiving the submission on December 8, 2023.

This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5160.

Submission Details

510(k) Number K233880 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 2023
Decision Date March 06, 2024
Days to Decision 89 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement

Device Classification

Product Code HGX — Pump, Breast, Powered
Device Class Class II - Special Controls
CFR Regulation 21 CFR 884.5160