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FDA 510(k)

AMPLAID A756 SCREENING ADMITTANCE METER

K-Number: K031978 · 2003-07-21

ApplicantAmplaid
Decision Date2003-07-21
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AMPLAID A756 SCREENING ADMITTANCE METER is the device name listed in this FDA 510(k) record. The listed applicant is Amplaid. It received FDA 510(k) clearance on 2003-07-21 under 510(k) number K031978. The device is classified under product code ETY. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPLAID A756 SCREENING ADMITTANCE METER?

AMPLAID A756 SCREENING ADMITTANCE METER is a medical device that received FDA 510(k) clearance on 2003-07-21. The listed applicant is Amplaid. The 510(k) number is K031978.

When did AMPLAID A756 SCREENING ADMITTANCE METER receive FDA 510(k) clearance?

AMPLAID A756 SCREENING ADMITTANCE METER received FDA 510(k) clearance on 2003-07-21, under 510(k) number K031978.

Who is the listed applicant for AMPLAID A756 SCREENING ADMITTANCE METER?

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

What is the FDA product code for AMPLAID A756 SCREENING ADMITTANCE METER?

The FDA product code for AMPLAID A756 SCREENING ADMITTANCE METER is ETY.

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Related Devices (Code: ETY)

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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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