PULSE CRP TEST— 510(k) K923768

Substantially Equivalent

Pulse Scientific, Inc.

FDA 510(k) clearance K923768 for PULSE CRP TEST, Substantially Equivalent on 1992-12-01. Applicant: Pulse Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Pulse Scientific, Inc.
Product code: Code DCK
Device class: Class 2
Regulation: 21 CFR 866.5270
Advisory panel: Immunology
Date received: 1992-07-28
Decision date: 1992-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, Ont., Canada, CA

Download summary PDF View on FDA.gov ↗

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More clearances from Pulse Scientific, Inc.

K923767 — PULSE IM RED CELL TEST1992-10-16
K923771 — PULSE RF TEST1992-10-05

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