DRAPES, BARRIER, STERILE PATIENT READY— 510(k) K760212

Name: FDA 510(k) clearance K760212
Creator: U.S. Food and Drug Administration
Published: 1976-08-11

Substantially Equivalent

Surgikos, Inc.

FDA 510(k) clearance K760212 for DRAPES, BARRIER, STERILE PATIENT READY, Substantially Equivalent on 1976-08-11. Applicant: Surgikos, Inc.. Device class: 2.

Clearance details

Applicant: Surgikos, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1976-07-12
Decision date: 1976-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KKX

view all

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 Surgikos, Inc.

view all

K875107 — HEALTH CARE EYE PROTECTION1988-03-21
K874653 — STERILE SURGICAL SCRUB BRUSH1987-12-30
K861441 — NEUTRALON SURGICAL GLOVES1986-05-30
K852870 — BARRIER SURGICAL GOWN1985-07-23
K822535 — CIDEX*DIALYZER DISINFECTING SOLUTION1982-09-30

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