Product code KOX— General, Plastic Surgery

FDA has cleared 12 devices under product code KOX between 1982 and 1994, filed by 11 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19941 clearance
• 19934 clearances
• 19922 clearances
• 19902 clearances
• 19891 clearance
• 19881 clearance
• 19821 clearance

• Smith & Nephew United, Inc.2 clearances
• The Healthcare Group Laboratories, Inc.1 clearance
• Stephens Scientific1 clearance
• Orange-Sol, Inc.1 clearance
• Medi-Flex Hospital Products, Inc.1 clearance
• Kemi Labs, Inc.1 clearance
• Elantec, Inc.1 clearance
• Convatec, A Division of E.R. Squibb & Sons1 clearance
• Coloplast Corp.1 clearance
• Chad Labs Corp.1 clearance

• K934790 — SEPP ADHESIVE REMOVERMedi-Flex Hospital Products, Inc.·1994-03-11
• K931933 — CHAD LABS ADHESIVE BANDAGE REMOVERChad Labs Corp.·1993-07-08
• K924976 — ALLKARE(TM) ADHESIVE REMOVER WIPEConvatec, A Division of E.R. Squibb & Sons·1993-04-20
• K924571 — MEDI-SOLOrange-Sol, Inc.·1993-04-06
• K925618 — 3M REMOVER LOTION PRODUCT NUMBER 86XX3M Health Care, Ltd.·1993-03-31
• K923351 — SKIN SUPPORT PREP PADColoplast Corp.·1992-09-14
• K915150 — REMOVE ADHESIVE REMOVERSmith & Nephew United, Inc.·1992-01-09
• K902009 — ELANTEC'S SURGICAL TAPE REMOVERElantec, Inc.·1990-08-29
• K895293 — KEMI LABS - ADHESIVE BANDAGE REMOVERKemi Labs, Inc.·1990-02-09
• K893603 — REMOVE ADHESIVE REMOVERSmith & Nephew United, Inc.·1989-07-14
• K881359 — DECALCIFYING SOLUTION IIStephens Scientific·1988-04-19
• K821162 — ADHESIVE REMOVERThe Healthcare Group Laboratories, Inc.·1982-05-14