DISC 120 TRANSPORTER— 510(k) K801391

Name: FDA 510(k) clearance K801391
Creator: U.S. Food and Drug Administration
Published: 1980-07-14

Substantially Equivalent

Travenol Laboratories, S.A.

FDA 510(k) clearance K801391 for DISC 120 TRANSPORTER, Substantially Equivalent on 1980-07-14. Applicant: Travenol Laboratories, S.A.. Device class: 1.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code JZW
Device class: Class 1
Regulation: 21 CFR 866.4540
Advisory panel: Immunology
Date received: 1980-06-13
Decision date: 1980-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JZW

view all

K001647 — BN PROSPEC SYSTEM2000-09-26
K761234 — BEHRING LASER NEPHELOMETER1990-06-07
K892223 — BEHRING NEPHELOMETER 1001989-05-04
K873401 — TURBOX1987-09-23
K873407 — RRT SYSTEM LASER REFLECTOMETER ANALYZER1987-09-23

More clearances from Travenol Laboratories, S.A.

view all

K874181 — BAXTER BEDSIDE SYSTEM1988-02-22
K873894 — CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE1987-11-05
K873873 — RESUBMITTED MICRON TRANSFUSION FILTER1987-10-22
K873984 — AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)1987-10-20
K872364 — HEMODIALYSIS (SPS), MODEL 550, CODE 5M13091987-10-13

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