CHEST CATHETERS/THORACIC CATHETERS— 510(k) K851048

Name: FDA 510(k) clearance K851048
Creator: U.S. Food and Drug Administration
Published: 1985-06-05

Substantially Equivalent

Medovations, Inc.

FDA 510(k) clearance K851048 for CHEST CATHETERS/THORACIC CATHETERS, Substantially Equivalent on 1985-06-05. Applicant: Medovations, Inc.. Device class: 1.

Clearance details

Applicant: Medovations, Inc.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1985-03-14
Decision date: 1985-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wauwatosa, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GBS

view all

K912645 — ATRIUMS PDR THORACIC CATHETER1991-09-13
K883887 — AXIOM ATRAUM WOUND DRAINS1989-02-17
K881873 — INTRODUCTION/DRAINAGE CATHETER & ACCESS1988-05-18
K880895 — URESIL WOUND DRAIN TROCAR1988-03-14
K880376 — NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP1988-02-16

More clearances from Medovations, Inc.

view all

K142068 — BULLDOG BIOPSY VALVE, OLYMPUS AND FUJINON; PENTAX COMPATIBLE; DISPOSABLE RRIGATING ADAPTOR, STERILE AND NON-STERILE2015-03-10
K002363 — MEDOVATIONS ESOPHAGEAL DILATOR2000-11-01
K972119 — MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX)1998-02-02
K924646 — OVER THE GUIDEWIRE DILATATION SYSTEM1994-12-05
K913678 — TROCAR CATHETER1991-12-16

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