SHEER GLYDE DAMS

Barrier, Std, Oral Sex

LOUISE C. MYERS

The following data is part of a premarket notification filed by Louise C. Myers with the FDA for Sheer Glyde Dams.

Pre-market Notification Details

• Device ID: K990067
• 510k Number: K990067
• Device Name: SHEER GLYDE DAMS
• Classification: Barrier, Std, Oral Sex
• Applicant: LOUISE C. MYERS 14808 N.E. 66TH ST. Redmond, WA 98052 -4712
• Contact: Louise C Myers
• Correspondent: Louise C Myers; LOUISE C. MYERS 14808 N.E. 66TH ST. Redmond, WA 98052 -4712
• Product Code: MSC
• CFR Regulation Number: 884.5300 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1999-01-08
• Decision Date: 1999-02-19
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
80726893115107	K990067	000
80726893114919	K990067	000