DIESSE CRP TEST KIT— 510(k) K854221

Substantially Equivalent

Marvic Interpharma, Inc.

FDA 510(k) clearance K854221 for DIESSE CRP TEST KIT, Substantially Equivalent on 1985-11-25. Applicant: Marvic Interpharma, Inc.. Device class: 2.

Clearance details

Applicant: Marvic Interpharma, Inc.
Product code: Code DCK
Device class: Class 2
Regulation: 21 CFR 866.5270
Advisory panel: Immunology
Date received: 1985-10-18
Decision date: 1985-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Harbor, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DCK

K242170 — K-ASSAY CRP (Ver.2)2025-04-18
K201256 — Procise CRP, ProciseDx Analyzer, ProciseDx Calibration Cartridge2022-11-04
K192028 — Yumizen C1200 CRP2020-06-25
K192118 — CRP Vario2019-11-08
K191993 — Yumizen C1200 CRP2019-10-03

More clearances from Marvic Interpharma, Inc.

K854223 — VES-TEC/VES-MATIC1986-04-04
K854222 — DIESSE RF TEST KIT1986-02-06

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