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FDA 510(k)

IV BAG PUMP

K-Number: K940657 · 1995-02-03

ApplicantI-Flow Corp.
Decision Date1995-02-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV BAG PUMP is the device name listed in this FDA 510(k) record. The listed applicant is I-Flow Corp.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K940657. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV BAG PUMP?

IV BAG PUMP is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is I-Flow Corp.. The 510(k) number is K940657.

When did IV BAG PUMP receive FDA 510(k) clearance?

IV BAG PUMP received FDA 510(k) clearance on 1995-02-03, under 510(k) number K940657.

Who is the listed applicant for IV BAG PUMP?

The FDA 510(k) record lists I-Flow Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IV BAG PUMP?

The FDA product code for IV BAG PUMP is FPA.

Other records listing I-Flow Corp. 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.

View all 41 devices →

Related Devices (Code: FPA)

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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