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FDA 510(k)

I-FLOW ELASTOMERIC PUMP

K-Number: K020862 · 2002-03-26

ApplicantI-Flow Corp.
Decision Date2002-03-26
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I-FLOW ELASTOMERIC 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 2002-03-26 under 510(k) number K020862. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I-FLOW ELASTOMERIC PUMP?

I-FLOW ELASTOMERIC PUMP is a medical device that received FDA 510(k) clearance on 2002-03-26. The listed applicant is I-Flow Corp.. The 510(k) number is K020862.

When did I-FLOW ELASTOMERIC PUMP receive FDA 510(k) clearance?

I-FLOW ELASTOMERIC PUMP received FDA 510(k) clearance on 2002-03-26, under 510(k) number K020862.

Who is the listed applicant for I-FLOW ELASTOMERIC 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 I-FLOW ELASTOMERIC PUMP?

The FDA product code for I-FLOW ELASTOMERIC PUMP is MEB.

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 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: MEB)

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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