Molnlycke Mepore Sterile Self-Adhesive

FDA 510(k) K830050 · Lada Intl., Inc.

Substantially Equivalent

510(k) numberK830050

Submission

Device name
Molnlycke Mepore Sterile Self-Adhesive
Applicant
Lada Intl., Inc.
Mchenry, IL, US
Received
January 10, 1983
Decision date
June 2, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
NAD – Dressing, Wound, Occlusive
Device class
Class I (low risk)
Regulation
21 CFR 878.4020
Specialty
General, Plastic Surgery

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More from Hospital Specialty Co.

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K872833Breathguard Apnea MonitorBZQ · Traditional 04/01/1988SE
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K830166Molnlycke Ete Sterile Non-Adherent DressNAB · Traditional 02/09/1983SE
K830051Molnlycke Mesalt Sterile DressingFRO · Traditional 01/26/1983SE
K812141Lic Obstetrical TableKNC · Traditional 08/25/1981SE
K812142Lic 180 Medical LampsKZF · Traditional 08/13/1981SE

Questions and answers

When was Molnlycke Mepore Sterile Self-Adhesive cleared by the FDA?

Molnlycke Mepore Sterile Self-Adhesive (K830050) received a 510(k) decision of Substantially Equivalent on June 2, 1983, 143 days after the submission was received.

What is the product code of K830050?

The FDA product code is NAD – Dressing, Wound, Occlusive, a Class I (low risk) device regulated under 21 CFR 878.4020.