DENTAL HANDPIECE

Handpiece, Air-powered, Dental

LARES MANUFACTURING CO., INC.

The following data is part of a premarket notification filed by Lares Manufacturing Co., Inc. with the FDA for Dental Handpiece.

Pre-market Notification Details

• Device ID: K780038
• 510k Number: K780038
• Device Name: DENTAL HANDPIECE
• Classification: Handpiece, Air-powered, Dental
• Applicant: LARES MANUFACTURING CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: EFB
• CFR Regulation Number: 872.4200 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1978-01-09
• Decision Date: 1978-01-20

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
D950100040	K780038	000