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FDA Product Code

FDA Product Code KOX — Clearance Directory

Device Class
Class I
21 CFR Citation
878.4730

510(k) Clearances — 12 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K934790 SEPP ADHESIVE REMOVER Medi-Flex Hospital Products, Inc. 1994-03-11 Traditional PDF ↗
K931933 CHAD LABS ADHESIVE BANDAGE REMOVER Chad Labs Corp. 1993-07-08 Traditional PDF ↗
K924976 ALLKARE(TM) ADHESIVE REMOVER WIPE Convatec, A Division of E.R. Squibb & Sons 1993-04-20 Traditional PDF ↗
K924571 MEDI-SOL Orange-Sol, Inc. 1993-04-06 Traditional PDF ↗
K925618 3M REMOVER LOTION PRODUCT NUMBER 86XX 3M Health Care, Ltd. 1993-03-31 Traditional PDF ↗
K923351 SKIN SUPPORT PREP PAD Coloplast Corp. 1992-09-14 Traditional PDF ↗
K915150 REMOVE ADHESIVE REMOVER Smith & Nephew United, Inc. 1992-01-09 Traditional PDF ↗
K902009 ELANTEC'S SURGICAL TAPE REMOVER Elantec, Inc. 1990-08-29 Traditional PDF ↗
K895293 KEMI LABS - ADHESIVE BANDAGE REMOVER Kemi Labs, Inc. 1990-02-09 Traditional PDF ↗
K893603 REMOVE ADHESIVE REMOVER Smith & Nephew United, Inc. 1989-07-14 Traditional PDF ↗
K881359 DECALCIFYING SOLUTION II Stephens Scientific 1988-04-19 Traditional PDF ↗
K821162 ADHESIVE REMOVER The Healthcare Group Laboratories, Inc. 1982-05-14 Traditional PDF ↗

Product code KOX · Class I · General, Plastic Surgery. Data: openFDA.