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FDA 510(k)

ARROW-JOHANS ECG ADAPTOR

K-Number: K843263 · 1984-09-20

ApplicantArrow Intl., Inc.
Decision Date1984-09-20
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW-JOHANS ECG ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1984-09-20 under 510(k) number K843263. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW-JOHANS ECG ADAPTOR?

ARROW-JOHANS ECG ADAPTOR is a medical device that received FDA 510(k) clearance on 1984-09-20. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K843263.

When did ARROW-JOHANS ECG ADAPTOR receive FDA 510(k) clearance?

ARROW-JOHANS ECG ADAPTOR received FDA 510(k) clearance on 1984-09-20, under 510(k) number K843263.

Who is the listed applicant for ARROW-JOHANS ECG ADAPTOR?

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

What is the FDA product code for ARROW-JOHANS ECG ADAPTOR?

The FDA product code for ARROW-JOHANS ECG ADAPTOR is DQY.

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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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