CHAD LABS ADHESIVE BANDAGE REMOVER
K-Number: K931933 · 1993-07-08
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Device Summary
Frequently Asked Questions
What is the CHAD LABS ADHESIVE BANDAGE REMOVER?
CHAD LABS ADHESIVE BANDAGE REMOVER is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Chad Labs Corp.. The 510(k) number is K931933.
When did CHAD LABS ADHESIVE BANDAGE REMOVER receive FDA 510(k) clearance?
CHAD LABS ADHESIVE BANDAGE REMOVER received FDA 510(k) clearance on 1993-07-08, under 510(k) number K931933.
Who is the listed applicant for CHAD LABS ADHESIVE BANDAGE REMOVER?
The FDA 510(k) record lists Chad Labs Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHAD LABS ADHESIVE BANDAGE REMOVER?
The FDA product code for CHAD LABS ADHESIVE BANDAGE REMOVER is KOX.
Related Clinical Trials
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.
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.
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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