FDA 510(k)

EZ PUMP

K-Number: K926446 · 1993-09-27

Decision Date1993-09-27

Product CodeFRW

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

EZ PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Alphamed, Inc.. It received FDA 510(k) clearance on 1993-09-27 under 510(k) number K926446. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ PUMP?

EZ PUMP is a medical device that received FDA 510(k) clearance on 1993-09-27. The listed applicant is Alphamed, Inc.. The 510(k) number is K926446.

When did EZ PUMP receive FDA 510(k) clearance?

EZ PUMP received FDA 510(k) clearance on 1993-09-27, under 510(k) number K926446.

Who is the listed applicant for EZ PUMP?

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

What is the FDA product code for EZ PUMP?

The FDA product code for EZ PUMP is FRW.

Other records listing Alphamed, 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.

K190210Tear Pool Dissolvable Punctum Plugs K091240ALPHAMED SURGICAL SPEAR, MODEL 70-5000 K990321ALPHAMED GEMINI SENSOR, SNORING SENSOR

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.