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FDA 510(k)

IV ALERT SYSTEM

K-Number: K820200 · 1982-03-18

ApplicantAllied Medical Technologies, Inc.
Decision Date1982-03-18
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV ALERT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Allied Medical Technologies, Inc.. It received FDA 510(k) clearance on 1982-03-18 under 510(k) number K820200. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV ALERT SYSTEM?

IV ALERT SYSTEM is a medical device that received FDA 510(k) clearance on 1982-03-18. The listed applicant is Allied Medical Technologies, Inc.. The 510(k) number is K820200.

When did IV ALERT SYSTEM receive FDA 510(k) clearance?

IV ALERT SYSTEM received FDA 510(k) clearance on 1982-03-18, under 510(k) number K820200.

Who is the listed applicant for IV ALERT SYSTEM?

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

What is the FDA product code for IV ALERT SYSTEM?

The FDA product code for IV ALERT SYSTEM is KPE.

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Related Devices (Code: KPE)

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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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