URIC ACID PAP— 510(k) K895665

Substantially Equivalent

Boehringer Mannheim Corp.

FDA 510(k) clearance K895665 for URIC ACID PAP, Substantially Equivalent on 1989-10-23. Applicant: Boehringer Mannheim Corp.. Device class: 1.

Clearance details

Applicant: Boehringer Mannheim Corp.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1989-09-20
Decision date: 1989-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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K984372 — ELECSYS CALCHECK TROPONIN T1998-12-14

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