FDA · official record K932932Substantially Equivalent

SNOREMASTER SNORE REMEDY

Name: SNOREMASTER SNORE REMEDY — FDA K932932
Creator: The Snoremaster Co.
Keywords: SNOREMASTER SNORE REMEDY, SNOREMASTER SNORE REMEDY, K932932, LQZ, FDA

United StatesLQZThe Snoremaster Co.

Verified

Official record identity

FDA application number: K932932
Decision date: February 10, 1995
Published decision: Substantially Equivalent

Classification

Product code: LQZ

Published parties

Applicant: The Snoremaster Co.

Additional source fields

Decision code: SESE
Published decision: Substantially Equivalent
Submission type: Traditional
Received date: 1993-06-16
Review panel: Dental
Current product-code class (harmonized): 2
Current product-code regulation (harmonized): 872.5570

About this record

This record preserves an application published in the FDA 510(k) bulk export, including the DEN entries FDA includes in that export. Historical decisions do not establish current marketing status. Product-code harmonization is separate from the original application; joined establishment identifiers are not assigned to the applicant. The complete official export is checked daily and raw evidence is retained.