HVA EIA KIT YAMASA— 510(k) K895288

Substantially Equivalent

Yamasa Shoy Co., Ltd.

FDA 510(k) clearance K895288 for HVA EIA KIT YAMASA, Substantially Equivalent on 1989-10-31. Applicant: Yamasa Shoy Co., Ltd.. Device class: 1.

Clearance details

Applicant: Yamasa Shoy Co., Ltd.
Product code: Code CDF
Device class: Class 1
Regulation: 21 CFR 862.1795
Advisory panel: Clinical Chemistry
Date received: 1989-08-25
Decision date: 1989-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chuoku, Tokyo 103 Japan, JP

Download summary PDF View on FDA.gov ↗

Recent devices under product code CDF

K953077 — PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM1996-01-05
K934977 — MODEL 5500 CEAS1994-01-11
K895287 — VMA EIA KIT YAMASA1989-10-30
K873372 — HVA & HOMOVANILLIC ACID BY HPLC METHOD1987-12-22
K861962 — VANILMANDELIC ACID (VMA) REAGENT SET1986-07-07

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