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FDA 510(k)

HOLLOW LUMEN NEEDLE, PART NUMBER: MX920

K-Number: K903199 · 1990-12-17

ApplicantMedex, Inc.
Decision Date1990-12-17
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HOLLOW LUMEN NEEDLE, PART NUMBER: MX920 is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K903199. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLLOW LUMEN NEEDLE, PART NUMBER: MX920?

HOLLOW LUMEN NEEDLE, PART NUMBER: MX920 is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is Medex, Inc.. The 510(k) number is K903199.

When did HOLLOW LUMEN NEEDLE, PART NUMBER: MX920 receive FDA 510(k) clearance?

HOLLOW LUMEN NEEDLE, PART NUMBER: MX920 received FDA 510(k) clearance on 1990-12-17, under 510(k) number K903199.

Who is the listed applicant for HOLLOW LUMEN NEEDLE, PART NUMBER: MX920?

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

What is the FDA product code for HOLLOW LUMEN NEEDLE, PART NUMBER: MX920?

The FDA product code for HOLLOW LUMEN NEEDLE, PART NUMBER: MX920 is DQO.

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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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