SNORING SENSOR— 510(k) K941759

Name: FDA 510(k) clearance K941759
Creator: U.S. Food and Drug Administration
Published: 1994-11-10

Substantially Equivalent - Subject to Tracking Reg.

Epm Development Systems Corp.

FDA 510(k) clearance K941759 for SNORING SENSOR, Substantially Equivalent - Subject to Tracking Reg. on 1994-11-10. Applicant: Epm Development Systems Corp.. Device class: 2.

Clearance details

Applicant: Epm Development Systems Corp.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1994-03-10
Decision date: 1994-11-10
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Traditional
Location: Midlothian, VA, US

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