DURATECH HOSPITAL TOWEL— 510(k) K920045

Substantially Equivalent

Techstyles

FDA 510(k) clearance K920045 for DURATECH HOSPITAL TOWEL, Substantially Equivalent on 1992-07-02. Applicant: Techstyles. Device class: 2.

Clearance details

Applicant: Techstyles
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1992-01-06
Decision date: 1992-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, 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 Techstyles

K992436 — GOWN BACK, MODEL 13-403N; 13-404N; 13-405N2000-01-20
K920153 — THERMUFF BAG1992-07-01

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