Molnlycke Mesalt Sterile Dressing

FDA 510(k) K830051 · Lada Intl., Inc.

Substantially Equivalent

510(k) numberK830051

Submission

Device name
Molnlycke Mesalt Sterile Dressing
Applicant
Lada Intl., Inc.
Walker, MI, US
Received
January 10, 1983
Decision date
January 26, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FRO – Dressing, Wound, Drug
Device class
Unclassified

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More from Solventum Germany GmbH

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K872833Breathguard Apnea MonitorBZQ · Traditional 04/01/1988SE
K861410Lic Mobile Transport StretchersFPO · Traditional 04/22/1986SE
K830050Molnlycke Mepore Sterile Self-AdhesiveNAD · Traditional 06/02/1983SE
K830166Molnlycke Ete Sterile Non-Adherent DressNAB · Traditional 02/09/1983SE
K812141Lic Obstetrical TableKNC · Traditional 08/25/1981SE
K812142Lic 180 Medical LampsKZF · Traditional 08/13/1981SE

Questions and answers

When was Molnlycke Mesalt Sterile Dressing cleared by the FDA?

Molnlycke Mesalt Sterile Dressing (K830051) received a 510(k) decision of Substantially Equivalent on January 26, 1983, 16 days after the submission was received.

What is the product code of K830051?

The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.