WHITE RIVER MINI MANUAL BREAST PUMP
K-Number: K971231 · 1997-05-19
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Device Summary
Frequently Asked Questions
What is the WHITE RIVER MINI MANUAL BREAST PUMP?
WHITE RIVER MINI MANUAL BREAST PUMP is a medical device that received FDA 510(k) clearance on 1997-05-19. The listed applicant is White River Concepts. The 510(k) number is K971231.
When did WHITE RIVER MINI MANUAL BREAST PUMP receive FDA 510(k) clearance?
WHITE RIVER MINI MANUAL BREAST PUMP received FDA 510(k) clearance on 1997-05-19, under 510(k) number K971231.
Who is the listed applicant for WHITE RIVER MINI MANUAL 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 MINI MANUAL BREAST PUMP?
The FDA product code for WHITE RIVER MINI MANUAL 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.
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: 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.
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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