VECTOR

Scaler, Ultrasonic

AIR TECHNIQUES, INC.

The following data is part of a premarket notification filed by Air Techniques, Inc. with the FDA for Vector.

Pre-market Notification Details

• Device ID: K002122
• 510k Number: K002122
• Device Name: VECTOR
• Classification: Scaler, Ultrasonic
• Applicant: AIR TECHNIQUES, INC. 70 CANTIAGUE ROCK RD. Hicksville, NY 11801
• Contact: Joseph Carey
• Correspondent: Joseph Carey; AIR TECHNIQUES, INC. 70 CANTIAGUE ROCK RD. Hicksville, NY 11801
• Product Code: ELC
• CFR Regulation Number: 872.4850 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2000-07-13
• Decision Date: 2000-12-21