PERIPHERAL PULSE FUNCTION BLOCKS— 510(k) K810171

Name: FDA 510(k) clearance K810171
Creator: U.S. Food and Drug Administration
Published: 1981-02-25

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K810171 for PERIPHERAL PULSE FUNCTION BLOCKS, Substantially Equivalent on 1981-02-25. Applicant: Honeywell, Inc.. Device class: 2.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1981-01-22
Decision date: 1981-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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