WHITE RIVER BATTERY-POWERED BREAST PUMP
K-Number: K952712 · 1996-04-18
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Device Summary
Frequently Asked Questions
What is the WHITE RIVER BATTERY-POWERED BREAST PUMP?
WHITE RIVER BATTERY-POWERED BREAST PUMP is a medical device that received FDA 510(k) clearance on 1996-04-18. The listed applicant is Natural Technologies, Inc.. The 510(k) number is K952712.
When did WHITE RIVER BATTERY-POWERED BREAST PUMP receive FDA 510(k) clearance?
WHITE RIVER BATTERY-POWERED BREAST PUMP received FDA 510(k) clearance on 1996-04-18, under 510(k) number K952712.
Who is the listed applicant for WHITE RIVER BATTERY-POWERED BREAST PUMP?
The FDA 510(k) record lists Natural Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WHITE RIVER BATTERY-POWERED BREAST PUMP?
The FDA product code for WHITE RIVER BATTERY-POWERED 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 Natural Technologies, 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.
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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