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FDA 510(k)

SMARTINFUSER PAINPUMP

K-Number: K042122 · 2004-09-22

Decision Date2004-09-22
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SMARTINFUSER PAINPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Precise Medical Products. It received FDA 510(k) clearance on 2004-09-22 under 510(k) number K042122. 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 SMARTINFUSER PAINPUMP?

SMARTINFUSER PAINPUMP is a medical device that received FDA 510(k) clearance on 2004-09-22. The listed applicant is Precise Medical Products. The 510(k) number is K042122.

When did SMARTINFUSER PAINPUMP receive FDA 510(k) clearance?

SMARTINFUSER PAINPUMP received FDA 510(k) clearance on 2004-09-22, under 510(k) number K042122.

Who is the listed applicant for SMARTINFUSER PAINPUMP?

The FDA 510(k) record lists Precise Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMARTINFUSER PAINPUMP?

The FDA product code for SMARTINFUSER PAINPUMP 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.

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

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

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