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FDA 510(k)

WHITE RIVER AUTOMATIC BREAST PUMP

K-Number: K964679 · 1997-06-10

Decision Date1997-06-10
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WHITE RIVER AUTOMATIC BREAST PUMP is the device name listed in this FDA 510(k) record. The listed applicant is White River Concepts. It received FDA 510(k) clearance on 1997-06-10 under 510(k) number K964679. 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 WHITE RIVER AUTOMATIC BREAST PUMP?

WHITE RIVER AUTOMATIC BREAST PUMP is a medical device that received FDA 510(k) clearance on 1997-06-10. The listed applicant is White River Concepts. The 510(k) number is K964679.

When did WHITE RIVER AUTOMATIC BREAST PUMP receive FDA 510(k) clearance?

WHITE RIVER AUTOMATIC BREAST PUMP received FDA 510(k) clearance on 1997-06-10, under 510(k) number K964679.

Who is the listed applicant for WHITE RIVER AUTOMATIC BREAST PUMP?

The FDA 510(k) record lists White River Concepts as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHITE RIVER AUTOMATIC BREAST PUMP?

The FDA product code for WHITE RIVER AUTOMATIC 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 White River Concepts 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.

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

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

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