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FDA 510(k)

QUALTEX TUBE/CORD ORGANIZER

K-Number: K921350 · 1992-08-04

ApplicantDeroyal Industries, Inc.
Decision Date1992-08-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

QUALTEX TUBE/CORD ORGANIZER is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1992-08-04 under 510(k) number K921350. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUALTEX TUBE/CORD ORGANIZER?

QUALTEX TUBE/CORD ORGANIZER is a medical device that received FDA 510(k) clearance on 1992-08-04. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K921350.

When did QUALTEX TUBE/CORD ORGANIZER receive FDA 510(k) clearance?

QUALTEX TUBE/CORD ORGANIZER received FDA 510(k) clearance on 1992-08-04, under 510(k) number K921350.

Who is the listed applicant for QUALTEX TUBE/CORD ORGANIZER?

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

What is the FDA product code for QUALTEX TUBE/CORD ORGANIZER?

The FDA product code for QUALTEX TUBE/CORD ORGANIZER is KKX.

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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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