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FDA 510(k)

ELANTEC'S SURGICAL TAPE REMOVER

K-Number: K902009 · 1990-08-29

ApplicantElantec, Inc.
Decision Date1990-08-29
Product CodeKOX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELANTEC'S SURGICAL TAPE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Elantec, Inc.. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K902009. 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 ELANTEC'S SURGICAL TAPE REMOVER?

ELANTEC'S SURGICAL TAPE REMOVER is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Elantec, Inc.. The 510(k) number is K902009.

When did ELANTEC'S SURGICAL TAPE REMOVER receive FDA 510(k) clearance?

ELANTEC'S SURGICAL TAPE REMOVER received FDA 510(k) clearance on 1990-08-29, under 510(k) number K902009.

Who is the listed applicant for ELANTEC'S SURGICAL TAPE REMOVER?

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

What is the FDA product code for ELANTEC'S SURGICAL TAPE REMOVER?

The FDA product code for ELANTEC'S SURGICAL TAPE REMOVER is KOX.

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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 & SonsK924571MEDI-SOLOrange-Sol, Inc.K9256183M REMOVER LOTION PRODUCT NUMBER 86XX3M Health Care, Ltd.K923351SKIN SUPPORT PREP PADColoplast Corp.

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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