Diagnostic Products Corp.
FDA 510(k) medical device clearances.
Clearances by Diagnostic Products Corp. — page 4
301–321 of 321- K810002 — 'NO-BOIL' VITAMIN B12 KIT
- K801580 — FERRITIN RIA KIT
- K800813 — DIAGNOSTIC PRODUCTS CORP. RIA CONTROL
- K792166 — 125 I PROLACTIN HORMONE RIA KIT
- K791405 — 125I LEUTINIZING HORMONE RIA KIT
- K790514 — I NETILMICIN RIA KIT
- K782126 — RIA KIT, SISOMICIN
- K782125 — RIA KIT, KANAMYCIN
- K780766 — (125 I) DIGITOXIN RIA KIT
- K780494 — AMIKACIN
- K780495 — DIGITOXIN
- K772191 — TESTOSTERONE RIA KIT (125I)
- K772192 — NEONATAL TSH RIA KIT (125I)
- K772188 — FSH RIA KIT (125I)
- K771525 — 125 I DIGOXIN RIA KIT
- K771526 — 125 I ALDOSTERONE RIA KIT
- K761157 — AMINOGLYCOSIDE (125I) RIA KIT
- K770241 — NEONATAL T4 RIA KIT
- K760967 — TOBRAMYCIN RIA KIT
- K760801 — TSH RIA KIT
- K760802 — T-3 UPTAKE KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.