MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT— 510(k) K895502

Name: FDA 510(k) clearance K895502
Creator: U.S. Food and Drug Administration
Published: 1989-12-08

Substantially Equivalent

Microbio-Medics, Inc.

FDA 510(k) clearance K895502 for MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT, Substantially Equivalent on 1989-12-08. Applicant: Microbio-Medics, Inc.. Device class: 1.

Clearance details

Applicant: Microbio-Medics, Inc.
Product code: Code EPP
Device class: Class 1
Regulation: 21 CFR 874.5800
Advisory panel: Ear, Nose, Throat
Date received: 1989-09-12
Decision date: 1989-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, MS, US

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