MEDI-SOL— 510(k) K924571

Substantially Equivalent

Orange-Sol, Inc.

FDA 510(k) clearance K924571 for MEDI-SOL, Substantially Equivalent on 1993-04-06. Applicant: Orange-Sol, Inc.. Device class: 1.

Clearance details

Applicant: Orange-Sol, Inc.
Product code: Code KOX
Device class: Class 1
Regulation: 21 CFR 878.4730
Advisory panel: General, Plastic Surgery
Date received: 1992-09-10
Decision date: 1993-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gilbert, AZ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KOX

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K931933 — CHAD LABS ADHESIVE BANDAGE REMOVER1993-07-08
K924976 — ALLKARE(TM) ADHESIVE REMOVER WIPE1993-04-20
K925618 — 3M REMOVER LOTION PRODUCT NUMBER 86XX1993-03-31
K923351 — SKIN SUPPORT PREP PAD1992-09-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.