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FDA 510(k)

RESUS-AID

K-Number: K881065 · 1988-07-14

ApplicantApplied Convergent Technologies, Inc.
Decision Date1988-07-14
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESUS-AID is the device name listed in this FDA 510(k) record. The listed applicant is Applied Convergent Technologies, Inc.. It received FDA 510(k) clearance on 1988-07-14 under 510(k) number K881065. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESUS-AID?

RESUS-AID is a medical device that received FDA 510(k) clearance on 1988-07-14. The listed applicant is Applied Convergent Technologies, Inc.. The 510(k) number is K881065.

When did RESUS-AID receive FDA 510(k) clearance?

RESUS-AID received FDA 510(k) clearance on 1988-07-14, under 510(k) number K881065.

Who is the listed applicant for RESUS-AID?

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

What is the FDA product code for RESUS-AID?

The FDA product code for RESUS-AID is CAE.

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Related Devices (Code: CAE)

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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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