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FDA 510(k)

MOLNLYCKE MESALT STERILE DRESSING

K-Number: K830051 · 1983-01-26

ApplicantLada Intl., Inc.
Decision Date1983-01-26
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

MOLNLYCKE MESALT STERILE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Lada Intl., Inc.. It received FDA 510(k) clearance on 1983-01-26 under 510(k) number K830051. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLNLYCKE MESALT STERILE DRESSING?

MOLNLYCKE MESALT STERILE DRESSING is a medical device that received FDA 510(k) clearance on 1983-01-26. The listed applicant is Lada Intl., Inc.. The 510(k) number is K830051.

When did MOLNLYCKE MESALT STERILE DRESSING receive FDA 510(k) clearance?

MOLNLYCKE MESALT STERILE DRESSING received FDA 510(k) clearance on 1983-01-26, under 510(k) number K830051.

Who is the listed applicant for MOLNLYCKE MESALT STERILE DRESSING?

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

What is the FDA product code for MOLNLYCKE MESALT STERILE DRESSING?

The FDA product code for MOLNLYCKE MESALT STERILE DRESSING is FRO. This falls under the Anesthesiology category.

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Other records listing Lada Intl., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K872833BREATHGUARD APNEA MONITORK861410LIC MOBILE TRANSPORT STRETCHERSK830050MOLNLYCKE MEPORE STERILE SELF-ADHESIVEK830166MOLNLYCKE ETE STERILE NON-ADHERENT DRESSK812141LIC OBSTETRICAL TABLEK812142LIC 180 MEDICAL LAMPS

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Related Devices (Code: FRO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, Inc.

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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