SUTURE REMOVAL KIT— 510(k) K920340

Unknown

Medikmark, Inc.

FDA 510(k) clearance K920340 for SUTURE REMOVAL KIT, Unknown on 1992-04-23. Applicant: Medikmark, Inc.. Device class: 2.

Clearance details

Applicant: Medikmark, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1992-01-24
Decision date: 1992-04-23
Decision: Unknown
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KKX

K230645 — BeneHold Surgical Incise Drape with CHG antimicrobial II2023-10-25
K222578 — 3M Ioban CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)2023-05-18
K202208 — BeneHold Surgical Incise Drape with CHG antimicrobial2021-07-30
K200238 — ControlRad Sterile Cover2020-04-26
K163556 — MediClear PreOp2017-09-14

More clearances from Medikmark, Inc.

K953474 — IV START KIT1995-10-02
K923960 — UPPER EXTERMITY DRAPE KIT1994-10-07
K921730 — C-SECTION PACK1994-06-15
K921732 — MINOR LAP SET1994-06-15
K921733 — TRACHEOSTOMY CARE TRAY1994-06-15

Data sourced from openFDA. This site is unofficial and independent of the FDA.