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FDA 510(k)

CHAD LABS ADHESIVE BANDAGE REMOVER

K-Number: K931933 · 1993-07-08

Decision Date1993-07-08
Product CodeKOX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHAD LABS ADHESIVE BANDAGE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Chad Labs Corp.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K931933. 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 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

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

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