IMPULSE 6000D/7000DP— 510(k) K072114

Substantially Equivalent

Fluke Biomedical

FDA 510(k) clearance K072114 for IMPULSE 6000D/7000DP, Substantially Equivalent on 2008-01-28. Applicant: Fluke Biomedical.

Clearance details

Applicant: Fluke Biomedical
Product code: Code DRL
Advisory panel: Cardiovascular
Date received: 2007-08-01
Decision date: 2008-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, CA, US

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