BETAFLO 2000— 510(k) K862273

Substantially Equivalent

Betaflo, Inc.

FDA 510(k) clearance K862273 for BETAFLO 2000, Substantially Equivalent on 1986-07-18. Applicant: Betaflo, Inc.. Device class: 2.

Clearance details

Applicant: Betaflo, Inc.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1986-06-16
Decision date: 1986-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

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