Organon Teknika Corp.
Organon Teknika Corp. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 2000.
Clearances by Organon Teknika Corp. — page 2
101–130 of 130- K854271 — ASA BLOOD TUBING LINES
- K854087 — NML TSH IRMA
- K853591 — DIALYZER, CAPILLARY, HOLLOW FIBER
- K851188 — PACKETS FOR PREP. OF DIALYSATES & INFUSATES -
- K844630 — ROPE SYSTEM REVERSE OSMOSIS PERITONEAL SYSTEM
- K850569 — BSM 2000 DIALYSIS MACHINE - MODIFIED
- K844748 — NEPHROSS ALLEGRO H.F.
- K843531 — ASN MONITOR SINGLE NEEDLE MONITOR
- K842513 — HEMOPERFUSION PROCEDURE W/REDY 2000
- K842302 — FLUID WARMER
- K842215 — ASCORBIC ACID
- K842154 — PACKETS FOR THE PREP OF DIALYSATES &
- K840062 — BSM 2000 DIALYSIS MACHINE
- K840743 — REDY 2000
- K832666 — NEPHROSS PRESTO
- K831641 — READER MICROELISA SYSTEM
- K831640 — WASHER 6000 MICRO-C LISA SYSTEM
- K831644 — PIPETTE 12 CHANNEL
- K831642 — HEATING BLOCK MICROELISA SYSTEM
- K831643 — STRIPREADER MICROELISA SYSTEM
- K831658 — MICROELISA COMP
- K823375 — NEPHROSS, ANDANTE H.F.
- K813574 — SORB II
- K812869 — D-3260 SORBENT CARTRIDGE
- K811170 — D-3160 SORBENT CARTRIDGE
- K802114 — NEPHROSS DIALYZER
- K802263 — MINIVISOR TERMINAL
- K801385 — K1 POTASSIUM ACETATE ADDITIVE
- K801440 — SORB 10 DIALYSATE INFUSATE C1 INFUSATE
- K792137 — SORB SYSTEM URS
Data sourced from openFDA. This site is unofficial and independent of the FDA.