B.A.C. 1000 MOBILE STANDING DEVICE— 510(k) K884840

Name: FDA 510(k) clearance K884840
Creator: U.S. Food and Drug Administration
Published: 1989-03-15

Substantially Equivalent

Luconex, Inc.

FDA 510(k) clearance K884840 for B.A.C. 1000 MOBILE STANDING DEVICE, Substantially Equivalent on 1989-03-15. Applicant: Luconex, Inc.. Device class: 2.

Clearance details

Applicant: Luconex, Inc.
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 1988-11-21
Decision date: 1989-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Foster City, CA, US

Download summary PDF View on FDA.gov ↗

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