SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR— 510(k) K973914

Name: FDA 510(k) clearance K973914
Creator: U.S. Food and Drug Administration
Published: 1998-06-30

Substantially Equivalent

Sense Technology, Inc.

FDA 510(k) clearance K973914 for SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR, Substantially Equivalent on 1998-06-30. Applicant: Sense Technology, Inc.. Device class: Unclassified.

Clearance details

Applicant: Sense Technology, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1997-10-14
Decision date: 1998-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

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