PHYSICIANS CHOICE SILICONE EAR PUTTY— 510(k) K823921

Name: FDA 510(k) clearance K823921
Creator: U.S. Food and Drug Administration
Published: 1983-03-28

Substantially Equivalent

Santa Barbara Medco, Inc.

FDA 510(k) clearance K823921 for PHYSICIANS CHOICE SILICONE EAR PUTTY, Substantially Equivalent on 1983-03-28. Applicant: Santa Barbara Medco, Inc.. Device class: 1.

Clearance details

Applicant: Santa Barbara Medco, Inc.
Product code: Code LDG
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1982-12-28
Decision date: 1983-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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