WAVE— 510(k) K973091

Substantially Equivalent

Southern Dental Industries, Inc.

FDA 510(k) clearance K973091 for WAVE, Substantially Equivalent on 1997-12-08. Applicant: Southern Dental Industries, Inc.. Device class: 2.

Clearance details

Applicant: Southern Dental Industries, Inc.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1997-08-18
Decision date: 1997-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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