DIESSE RF TEST KIT— 510(k) K854222

Substantially Equivalent

Marvic Interpharma, Inc.

FDA 510(k) clearance K854222 for DIESSE RF TEST KIT, Substantially Equivalent on 1986-02-06. Applicant: Marvic Interpharma, Inc.. Device class: 2.

Clearance details

Applicant: Marvic Interpharma, Inc.
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1985-10-18
Decision date: 1986-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Harbor, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DHR

K192727 — K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2)2020-05-20
K190088 — QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents2019-04-17
K182747 — EliA RF IgM Immunoassay2018-12-18
K162263 — Optilite Rheumatoid Factor Kit2017-05-03
K160070 — Rheumatoid Factor (RF) Kit for use on SPAPLUS2016-12-07

More clearances from Marvic Interpharma, Inc.

K854223 — VES-TEC/VES-MATIC1986-04-04
K854221 — DIESSE CRP TEST KIT1985-11-25

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