AXIOM ATRAUM WOUND DRAINS— 510(k) K883887

Substantially Equivalent

Axiom, Inc.

FDA 510(k) clearance K883887 for AXIOM ATRAUM WOUND DRAINS, Substantially Equivalent on 1989-02-17. Applicant: Axiom, Inc.. Device class: 1.

Clearance details

Applicant: Axiom, Inc.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1988-09-13
Decision date: 1989-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paramount, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GBS

K912645 — ATRIUMS PDR THORACIC CATHETER1991-09-13
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
K873377 — CLOSED CHEST DRAINAGE SET W/SUTURES1987-10-28

More clearances from Axiom, Inc.

K842443 — AXIOM STABLE II TRIGLYCERIDES TEST1984-09-13
K842442 — AXIOM STABLE II URIC ACID TEST1984-08-16
K842441 — AXIOM STABLE II CHOLESTEROL TEST1984-07-25

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