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FDA 510(k)

AVIA PAIN MEDICATION DELIVERY SYSTEM

K-Number: K990312 · 1999-04-22

ApplicantAmtec Medical
Decision Date1999-04-22
Product CodeMEA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AVIA PAIN MEDICATION DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Amtec Medical. It received FDA 510(k) clearance on 1999-04-22 under 510(k) number K990312. 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 AVIA PAIN MEDICATION DELIVERY SYSTEM?

AVIA PAIN MEDICATION DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-22. The listed applicant is Amtec Medical. The 510(k) number is K990312.

When did AVIA PAIN MEDICATION DELIVERY SYSTEM receive FDA 510(k) clearance?

AVIA PAIN MEDICATION DELIVERY SYSTEM received FDA 510(k) clearance on 1999-04-22, under 510(k) number K990312.

Who is the listed applicant for AVIA PAIN MEDICATION DELIVERY SYSTEM?

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

What is the FDA product code for AVIA PAIN MEDICATION DELIVERY SYSTEM?

The FDA product code for AVIA PAIN MEDICATION DELIVERY SYSTEM is MEA.

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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.

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