BIOSPAL 2400S— 510(k) K834579

Substantially Equivalent

Hospal Medical Corp.

FDA 510(k) clearance K834579 for BIOSPAL 2400S, Substantially Equivalent on 1984-02-04. Applicant: Hospal Medical Corp.. Device class: 1.

Clearance details

Applicant: Hospal Medical Corp.
Product code: Code KDT
Device class: Class 1
Regulation: 21 CFR 864.3250
Advisory panel: Pathology
Date received: 1983-12-29
Decision date: 1984-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code KDT

K873593 — BIOSURE SPECIMEN COLLECTION CONTAINER1987-11-25
K862665 — NOVACYTE-U1986-09-04
K834412 — PRESERV PVA FIXATIVE 15ML-FORMALIN PK1984-01-13
K833660 — PRESERV PVA FIXATIVE -MALIN PACK1983-11-28
K823773 — PROVIAL II #006-010-02011983-01-21

More clearances from Hospal Medical Corp.

K893742 — FILTRAL TM 20 HEMODIALYZER/FILTER1989-07-24
K884365 — MULTIFLOW(TM) 60 KIT1988-12-08
K884326 — FILTRAL TM 8 HEMODIALYZER1988-12-05
K883307 — CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KIT1988-10-12
K872767 — FILTRAL 10, FILTRAL 12, FILTRAL 16 HEMODIALYZER1987-12-29

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