FDA 510(k)

KLEENIT BY QMED

K-Number: K843559 · 1984-10-24

Decision Date1984-10-24

Product Code

DecisionSubstantially Equivalent

Device Summary

KLEENIT BY QMED is the device name listed in this FDA 510(k) record. The listed applicant is Qmed, Inc.. It received FDA 510(k) clearance on 1984-10-24 under 510(k) number K843559. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLEENIT BY QMED?

KLEENIT BY QMED is a medical device that received FDA 510(k) clearance on 1984-10-24. The listed applicant is Qmed, Inc.. The 510(k) number is K843559.

When did KLEENIT BY QMED receive FDA 510(k) clearance?

KLEENIT BY QMED received FDA 510(k) clearance on 1984-10-24, under 510(k) number K843559.

Who is the listed applicant for KLEENIT BY QMED?

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

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Other records listing Qmed, 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.