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FDA 510(k)

PLAYTEX BREAST PUMP

K-Number: K022594 · 2002-11-01

Decision Date2002-11-01
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PLAYTEX BREAST PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Playtex Products, Inc.. It received FDA 510(k) clearance on 2002-11-01 under 510(k) number K022594. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAYTEX BREAST PUMP?

PLAYTEX BREAST PUMP is a medical device that received FDA 510(k) clearance on 2002-11-01. The listed applicant is Playtex Products, Inc.. The 510(k) number is K022594.

When did PLAYTEX BREAST PUMP receive FDA 510(k) clearance?

PLAYTEX BREAST PUMP received FDA 510(k) clearance on 2002-11-01, under 510(k) number K022594.

Who is the listed applicant for PLAYTEX BREAST PUMP?

The FDA 510(k) record lists Playtex Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLAYTEX BREAST PUMP?

The FDA product code for PLAYTEX BREAST PUMP is HGX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Playtex Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 17 devices →

Related Devices (Code: HGX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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