PLATELET ROTATOR— 510(k) K780189

Substantially Equivalent

Travenol Laboratories, S.A.

FDA 510(k) clearance K780189 for PLATELET ROTATOR, Substantially Equivalent on 1978-03-30. Applicant: Travenol Laboratories, S.A.. Device class: 1.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code KSQ
Device class: Class 1
Regulation: 21 CFR 864.9195
Advisory panel: Hematology
Date received: 1978-02-06
Decision date: 1978-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KSQ

K842746 — HYCEL ROTOR-MIXER AND/OR MULTI1984-08-17
K820712 — SEPCOR UNIT COLLECTION MONITOR1982-05-07
K812533 — PLATELET AGITATOR1981-09-29
K810617 — MOBILE MATIC AUTOMATIC DONOR SCALE1981-04-07
K802608 — HEMATIC BLOOD MIXER1980-12-11

More clearances from Travenol Laboratories, S.A.

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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.