FDA 510(k)

MEDI-SOL

K-Number: K924571 · 1993-04-06

Decision Date1993-04-06

Product CodeKOX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MEDI-SOL is the device name listed in this FDA 510(k) record. The listed applicant is Orange-Sol, Inc.. It received FDA 510(k) clearance on 1993-04-06 under 510(k) number K924571. The device is classified under product code KOX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-SOL?

MEDI-SOL is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Orange-Sol, Inc.. The 510(k) number is K924571.

When did MEDI-SOL receive FDA 510(k) clearance?

MEDI-SOL received FDA 510(k) clearance on 1993-04-06, under 510(k) number K924571.

Who is the listed applicant for MEDI-SOL?

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

What is the FDA product code for MEDI-SOL?

The FDA product code for MEDI-SOL is KOX.

Related Devices (Code: KOX)

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.

K934790SEPP ADHESIVE REMOVERMedi-Flex Hospital Products, Inc.K931933CHAD LABS ADHESIVE BANDAGE REMOVERChad Labs Corp.K924976ALLKARE(TM) ADHESIVE REMOVER WIPEConvatec, A Division of E.R. Squibb & Sons K9256183M REMOVER LOTION PRODUCT NUMBER 86XX3M Health Care, Ltd.K923351SKIN SUPPORT PREP PADColoplast Corp.K915150REMOVE ADHESIVE REMOVERSmith & Nephew United, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.