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BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081550
510(k) Type
Traditional
Applicant
BONART CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2008
Days to Decision
86 days
Submission Type
Statement

BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081550
510(k) Type
Traditional
Applicant
BONART CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2008
Days to Decision
86 days
Submission Type
Statement