PHOSPHORUS— 510(k) K895999

Substantially Equivalent

American Monitor Corp.

FDA 510(k) clearance K895999 for PHOSPHORUS, Substantially Equivalent on 1990-01-11. Applicant: American Monitor Corp.. Device class: 1.

Clearance details

Applicant: American Monitor Corp.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1989-10-13
Decision date: 1990-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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More clearances from American Monitor Corp.

K896000 — ASPARTATE AMINOTRANFERASE (AST)1990-01-11
K896001 — ALANINE AMINOTRANSFERASE (ALT)1989-11-13
K895423 — ACCESS CHEMISTRY ANALYZER1989-10-04
K893137 — EXCEL (TM) CHEMISTRY ANALYZER1989-08-10
K892331 — ENZYMATIC UREA NITROGEN REAGENT SET1989-06-20

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