BOUNDARY FABRIC III SURGICAL DRAPE— 510(k) K760932

Name: FDA 510(k) clearance K760932
Creator: U.S. Food and Drug Administration
Published: 1976-11-11

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K760932 for BOUNDARY FABRIC III SURGICAL DRAPE, Substantially Equivalent on 1976-11-11. Applicant: Procter & Gamble Mfg. Co.. Device class: 2.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1976-10-29
Decision date: 1976-11-11
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 Procter & Gamble Mfg. Co.

view all

K873036 — ATTENDS INCONTINENT BRIEF1988-01-19
K873457 — SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS1988-01-19
K864673 — UNSCENTED MENSTRUAL PAD1987-01-21
K861863 — MODIFIED PROTECTIVE GARMENT1986-08-11
K862348 — SINGLE-USE PATIENT UNDERPAD1986-07-02

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