MOI-STIR

Saliva, Artificial

KINGSWOOD LABORATORIES, INC.

The following data is part of a premarket notification filed by Kingswood Laboratories, Inc. with the FDA for Moi-stir.

Pre-market Notification Details

• Device ID: K810157
• 510k Number: K810157
• Device Name: MOI-STIR
• Classification: Saliva, Artificial
• Applicant: KINGSWOOD LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: LFD
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1981-01-21
• Decision Date: 1981-02-10

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00355299601040	K810157	000
00304369600421	K810157	000