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FDA 510(k)

ENTERNAL FEEDING PUMP BATTERY OPER.

K-Number: K841104 · 1985-04-30

ApplicantFresenius USA, Inc.
Decision Date1985-04-30
Product Code
DecisionSubstantially Equivalent

Device Summary

ENTERNAL FEEDING PUMP BATTERY OPER. is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius USA, Inc.. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K841104. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENTERNAL FEEDING PUMP BATTERY OPER.?

ENTERNAL FEEDING PUMP BATTERY OPER. is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Fresenius USA, Inc.. The 510(k) number is K841104.

When did ENTERNAL FEEDING PUMP BATTERY OPER. receive FDA 510(k) clearance?

ENTERNAL FEEDING PUMP BATTERY OPER. received FDA 510(k) clearance on 1985-04-30, under 510(k) number K841104.

Who is the listed applicant for ENTERNAL FEEDING PUMP BATTERY OPER.?

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

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Other records listing Fresenius USA, 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.

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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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