P.O. VOX— 510(k) K860993

Name: FDA 510(k) clearance K860993
Creator: U.S. Food and Drug Administration
Published: 1986-04-25

Substantially Equivalent

Bloomfield Research and Development, Inc.

FDA 510(k) clearance K860993 for P.O. VOX, Substantially Equivalent on 1986-04-25. Applicant: Bloomfield Research and Development, Inc.. Device class: 1.

Clearance details

Applicant: Bloomfield Research and Development, Inc.
Product code: Code ESE
Device class: Class 1
Regulation: 21 CFR 874.3375
Advisory panel: Ear, Nose, Throat
Date received: 1986-03-17
Decision date: 1986-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hilton Head, SC, US

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K860994 — DECITEL AUSCULSCOPE1986-11-07
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