THERAPACER 3000— 510(k) K925666

Substantially Equivalent

Kvm Technologies, Inc.

FDA 510(k) clearance K925666 for THERAPACER 3000, Substantially Equivalent on 1993-03-09. Applicant: Kvm Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Kvm Technologies, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1992-11-10
Decision date: 1993-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.