Molnlycke Mesalt Sterile Dressing
FDA 510(k) K830051 · Lada Intl., Inc.
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)
Device classification
- Product code
- FRO – Dressing, Wound, Drug
- Device class
- Unclassified
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More from Solventum Germany GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K872833 | Breathguard Apnea MonitorBZQ · Traditional | 04/01/1988SE |
| K861410 | Lic Mobile Transport StretchersFPO · Traditional | 04/22/1986SE |
| K830050 | Molnlycke Mepore Sterile Self-AdhesiveNAD · Traditional | 06/02/1983SE |
| K830166 | Molnlycke Ete Sterile Non-Adherent DressNAB · Traditional | 02/09/1983SE |
| K812141 | Lic Obstetrical TableKNC · Traditional | 08/25/1981SE |
| K812142 | Lic 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.