FDA 510(k)

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

K-Number: K020418 · 2003-04-29

Decision Date2003-04-29

Product CodeMEA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is P.T. Greenleaf. It received FDA 510(k) clearance on 2003-04-29 under 510(k) number K020418. The device is classified under product code MEA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES?

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES is a medical device that received FDA 510(k) clearance on 2003-04-29. The listed applicant is P.T. Greenleaf. The 510(k) number is K020418.

When did GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES receive FDA 510(k) clearance?

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES received FDA 510(k) clearance on 2003-04-29, under 510(k) number K020418.

Who is the listed applicant for GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES?

The FDA 510(k) record lists P.T. Greenleaf as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES?

The FDA product code for GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES is MEA.

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K020419V SET

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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.