TISSUE CULTURE FLASK PL 732 PLASTIC— 510(k) K861253

Name: FDA 510(k) clearance K861253
Creator: U.S. Food and Drug Administration
Published: 1986-04-11

Substantially Equivalent

Travenol Laboratories, S.A.

FDA 510(k) clearance K861253 for TISSUE CULTURE FLASK PL 732 PLASTIC, Substantially Equivalent on 1986-04-11. Applicant: Travenol Laboratories, S.A.. Device class: 1.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code KJA
Device class: Class 1
Regulation: 21 CFR 864.2240
Advisory panel: Hematology
Date received: 1986-04-03
Decision date: 1986-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerfield, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KJA

view all

K972404 — VACUTAINER BRAND SAFETY BLOOD COLLECTION ASSEMBLY(MULTIPLE)1997-07-22
K933228 — KAPTON PEEL POUCH1994-03-30
K885121 — CELL SCRAPER1988-12-28
K873889 — TISSUE CULTURE TUBES1987-11-25
K873890 — TISSUE CULTURE FLASKS1987-11-25

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.