LIQUISOL PROGESTERONE RADIOIMMUNO— 510(k) K820686

Substantially Equivalent

Damon Corp.

FDA 510(k) clearance K820686 for LIQUISOL PROGESTERONE RADIOIMMUNO, Substantially Equivalent on 1982-04-01. Applicant: Damon Corp.. Device class: 1.

Clearance details

Applicant: Damon Corp.
Product code: Code JLS
Device class: Class 1
Regulation: 21 CFR 862.1620
Advisory panel: Clinical Chemistry
Date received: 1982-03-11
Decision date: 1982-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Damon Corp.

K874865 — DAMON D.E.T.E.C.T IMAGE ENHANCER1987-12-23
K831826 — ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY1983-07-18
K802661 — LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT1980-12-10
K790250 — LIQUISOL CORTISOL RIA TEST KIT1979-04-04
K782124 — IEC CENTRA-7 CENTRIFUGE MODEL 23621979-02-26

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