B&L L-BETA, MODEL WL-B1— 510(k) K060347

Substantially Equivalent

B&L Biotech Co., Ltd.

FDA 510(k) clearance K060347 for B&L L-BETA, MODEL WL-B1, Substantially Equivalent on 2006-06-05. Applicant: B&L Biotech Co., Ltd.. Device class: 1.

Clearance details

Applicant: B&L Biotech Co., Ltd.
Product code: Code EKR
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 2006-02-10
Decision date: 2006-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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