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FDA 510(k)

RODY BREAST PUMP

K-Number: K840874 · 1984-07-23

ApplicantKean-Rody Manufacturer
Decision Date1984-07-23
Product CodeHGY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RODY BREAST PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Kean-Rody Manufacturer. It received FDA 510(k) clearance on 1984-07-23 under 510(k) number K840874. The device is classified under product code HGY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RODY BREAST PUMP?

RODY BREAST PUMP is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Kean-Rody Manufacturer. The 510(k) number is K840874.

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

RODY BREAST PUMP received FDA 510(k) clearance on 1984-07-23, under 510(k) number K840874.

Who is the listed applicant for RODY BREAST PUMP?

The FDA 510(k) record lists Kean-Rody Manufacturer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RODY BREAST PUMP?

The FDA product code for RODY BREAST PUMP is HGY.

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.

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Related Devices (Code: HGY)

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.

K101538HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)Philips Electronics UK LimitedK032845EASY COMFORT DELUXE MANUAL BREAST PUMP, MODEL 1187The First Years, Inc.K013226EVENFLO COMFORT EASE MANUAL BREAST PUMP KITEvenflo Company, Inc.K011519AMEDA HYGIENIKITHollister, Inc.K971231WHITE RIVER MINI MANUAL BREAST PUMPWhite River ConceptsK962828EVERT-ITGenesis Industries, Inc.

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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