RIA TEST, NORDICALB HPL— 510(k) K782099

Substantially Equivalent

Nordiclab Intl.

FDA 510(k) clearance K782099 for RIA TEST, NORDICALB HPL, Substantially Equivalent on 1979-01-10. Applicant: Nordiclab Intl.. Device class: 2.

Clearance details

Applicant: Nordiclab Intl.
Product code: Code JMF
Device class: Class 2
Regulation: 21 CFR 862.1585
Advisory panel: Clinical Chemistry
Date received: 1978-12-18
Decision date: 1979-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JMF

K944933 — IMMULITE (HPL) (HUMAN PLACENTAL PLACTOGEN)1995-03-10
K840588 — AMERLEX HUMAN PLACENTAL LACTOGEN1984-04-04
K823292 — IMMOPHASE TM HPL RADIOIMMUNOASSAY1982-12-28
K823201 — HUMAN PLACENTAL LACTOGEN KIT1982-11-29
K811370 — NATAL-TEC HPL1981-05-29

More clearances from Nordiclab Intl.

K801988 — NORDICLAB PROSTATIC ACID PHOSPHATASE RIA1980-09-26
K801989 — NORDICLAB FERRITIN IRMA TEST1980-09-16
K800920 — NORDICLAB ESTRADIOL RIA TEST1980-05-14
K800921 — NORDICLAB TESTOSTERONE RIA TEST1980-05-14
K800922 — NORDICLAB PROGESTERONE RIA TEST1980-05-14

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