CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM— 510(k) K934072

Name: FDA 510(k) clearance K934072
Creator: U.S. Food and Drug Administration
Published: 1994-09-08

Unknown

Contour Fabricators of Florida, Inc.

FDA 510(k) clearance K934072 for CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM, Unknown on 1994-09-08. Applicant: Contour Fabricators of Florida, Inc.. Device class: 2.

Clearance details

Applicant: Contour Fabricators of Florida, Inc.
Product code: Code KNY
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1993-08-20
Decision date: 1994-09-08
Decision: Unknown
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNY

view all

K260919 — Transurethral Catheter Safety Valve (TUCSV) (80050)2026-08-05
K182144 — Bi-Flex Evo2018-09-07
K162356 — Vesair Cystoscopic Sheath2017-03-02
K140441 — BI-FLEX URETERAL ACCESS SHEATH2014-06-17
K140562 — WIJAY EZ-VOID EXTERNAL CATHETER VALVE2014-06-16

More clearances from Contour Fabricators of Florida, Inc.

view all

K955685 — RNS STERILE, DISPOSABLE CT BIOPSY TRAY1996-10-04
K962040 — RNS ARTHROGRAM TRAY1996-06-25
K955687 — RNS STERILE, DISPOSABLE RADIOGRAPHIC CONTRAST TRAY1996-06-03
K955689 — RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY1996-05-15
K955684 — RNS STERILE, DISPOSABLE ANGIOGRAPHIC TRAY1996-05-02

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