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FDA 510(k)

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN

K-Number: K842342 · 1984-06-14

ApplicantMed-West, Inc.
Decision Date1984-06-14
Product Code
DecisionUnknown

Device Summary

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN is the device name listed in this FDA 510(k) record. The listed applicant is Med-West, Inc.. It received FDA 510(k) clearance on 1984-06-14 under 510(k) number K842342. FDA Decision: Unknown.

Frequently Asked Questions

What is the MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN?

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN is a medical device that received FDA 510(k) clearance on 1984-06-14. The listed applicant is Med-West, Inc.. The 510(k) number is K842342.

When did MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN receive FDA 510(k) clearance?

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN received FDA 510(k) clearance on 1984-06-14, under 510(k) number K842342.

Who is the listed applicant for MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN?

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

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Other records listing Med-West, 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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