Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALLKARE(TM) ADHESIVE REMOVER WIPE

K-Number: K924976 · 1993-04-20

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1993-04-20
Product CodeKOX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALLKARE(TM) ADHESIVE REMOVER WIPE is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K924976. 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 ALLKARE(TM) ADHESIVE REMOVER WIPE?

ALLKARE(TM) ADHESIVE REMOVER WIPE is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K924976.

When did ALLKARE(TM) ADHESIVE REMOVER WIPE receive FDA 510(k) clearance?

ALLKARE(TM) ADHESIVE REMOVER WIPE received FDA 510(k) clearance on 1993-04-20, under 510(k) number K924976.

Who is the listed applicant for ALLKARE(TM) ADHESIVE REMOVER WIPE?

The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLKARE(TM) ADHESIVE REMOVER WIPE?

The FDA product code for ALLKARE(TM) ADHESIVE REMOVER WIPE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Convatec, A Division of E.R. Squibb & Sons as applicant

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.

K013814ABSORBENT ANTIMICROBIAL WOUND DRESSINGK990964SIGNADRESS DUODERM DRESSINGK984388HA ABSORBENT WOUND DRESSINGK980720NONWOVEN PADK980382NON-WOVEN COMPRESSK974823NONWOVEN DRESSING

View all 81 devices →

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.K924571MEDI-SOLOrange-Sol, Inc.K9256183M REMOVER LOTION PRODUCT NUMBER 86XX3M Health Care, Ltd.K923351SKIN SUPPORT PREP PADColoplast Corp.K915150REMOVE ADHESIVE REMOVERSmith & Nephew United, Inc.

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.

↑