GREENLEAF SMART POLYGRAPH PROGRAM— 510(k) K854355

Name: FDA 510(k) clearance K854355
Creator: U.S. Food and Drug Administration
Published: 1986-04-18

Substantially Equivalent

Greenleaf Science Corp.

FDA 510(k) clearance K854355 for GREENLEAF SMART POLYGRAPH PROGRAM, Substantially Equivalent on 1986-04-18. Applicant: Greenleaf Science Corp.. Device class: 2.

Clearance details

Applicant: Greenleaf Science Corp.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1985-10-29
Decision date: 1986-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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