MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)— 510(k) K900731

Name: FDA 510(k) clearance K900731
Creator: U.S. Food and Drug Administration
Published: 1990-12-17

Substantially Equivalent

Medical Consultants Intl. , Ltd.

FDA 510(k) clearance K900731 for MEDI LISS DENTAL ANALGESIA DEVICE (SBL601), Substantially Equivalent on 1990-12-17. Applicant: Medical Consultants Intl. , Ltd.. Device class: Unclassified.

Clearance details

Applicant: Medical Consultants Intl. , Ltd.
Product code: Code LWM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1990-02-15
Decision date: 1990-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Rock, NJ, US

Download summary PDF View on FDA.gov ↗

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