FDA 510(k)

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

K-Number: K972158 · 1998-02-20

Decision Date1998-02-20

Product CodeMEB

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 Princeton Regulatory Assoc.. It received FDA 510(k) clearance on 1998-02-20 under 510(k) number K972158. 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 GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES?

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES is a medical device that received FDA 510(k) clearance on 1998-02-20. The listed applicant is Princeton Regulatory Assoc.. The 510(k) number is K972158.

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 1998-02-20, under 510(k) number K972158.

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

The FDA 510(k) record lists Princeton Regulatory Assoc. 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 MEB.

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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.