LS-100

Handpiece, Air-powered, Dental

MIDWEST

The following data is part of a premarket notification filed by Midwest with the FDA for Ls-100.

Pre-market Notification Details

• Device ID: K792302
• 510k Number: K792302
• Device Name: LS-100
• Classification: Handpiece, Air-powered, Dental
• Applicant: MIDWEST 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: 1979-11-16
• Decision Date: 1979-11-27

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
E276760034D0	K792302	000
E276710024D0	K792302	000