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FDA 510(k)

ARC ADAPTER ASSEMBLY

K-Number: K874833 · 1988-03-03

ApplicantMedical Equipment Development Co., Inc.
Decision Date1988-03-03
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ARC ADAPTER ASSEMBLY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Development Co., Inc.. It received FDA 510(k) clearance on 1988-03-03 under 510(k) number K874833. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARC ADAPTER ASSEMBLY?

ARC ADAPTER ASSEMBLY is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Medical Equipment Development Co., Inc.. The 510(k) number is K874833.

When did ARC ADAPTER ASSEMBLY receive FDA 510(k) clearance?

ARC ADAPTER ASSEMBLY received FDA 510(k) clearance on 1988-03-03, under 510(k) number K874833.

Who is the listed applicant for ARC ADAPTER ASSEMBLY?

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

What is the FDA product code for ARC ADAPTER ASSEMBLY?

The FDA product code for ARC ADAPTER ASSEMBLY is HAW.

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Other records listing Medical Equipment Development Co., Inc. as applicant

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Official Source

View on FDA Database →

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

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