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FDA 510(k)

KEMI LABS - ADHESIVE BANDAGE REMOVER

K-Number: K895293 · 1990-02-09

Decision Date1990-02-09
Product CodeKOX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KEMI LABS - ADHESIVE BANDAGE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Kemi Labs, Inc.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K895293. 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 KEMI LABS - ADHESIVE BANDAGE REMOVER?

KEMI LABS - ADHESIVE BANDAGE REMOVER is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Kemi Labs, Inc.. The 510(k) number is K895293.

When did KEMI LABS - ADHESIVE BANDAGE REMOVER receive FDA 510(k) clearance?

KEMI LABS - ADHESIVE BANDAGE REMOVER received FDA 510(k) clearance on 1990-02-09, under 510(k) number K895293.

Who is the listed applicant for KEMI LABS - ADHESIVE BANDAGE REMOVER?

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

What is the FDA product code for KEMI LABS - ADHESIVE BANDAGE REMOVER?

The FDA product code for KEMI 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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