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FDA 510(k)

ARROW M.I.S. MULTI-LUMEN CATHETERIZA

K-Number: K820648 · 1982-04-14

ApplicantArrow Intl., Inc.
Decision Date1982-04-14
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW M.I.S. MULTI-LUMEN CATHETERIZA 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 1982-04-14 under 510(k) number K820648. 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 M.I.S. MULTI-LUMEN CATHETERIZA?

ARROW M.I.S. MULTI-LUMEN CATHETERIZA is a medical device that received FDA 510(k) clearance on 1982-04-14. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K820648.

When did ARROW M.I.S. MULTI-LUMEN CATHETERIZA receive FDA 510(k) clearance?

ARROW M.I.S. MULTI-LUMEN CATHETERIZA received FDA 510(k) clearance on 1982-04-14, under 510(k) number K820648.

Who is the listed applicant for ARROW M.I.S. MULTI-LUMEN CATHETERIZA?

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 M.I.S. MULTI-LUMEN CATHETERIZA?

The FDA product code for ARROW M.I.S. MULTI-LUMEN CATHETERIZA is DQY.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: DQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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