NON-INVASIVE TUBING— 510(k) K921450

Name: FDA 510(k) clearance K921450
Creator: U.S. Food and Drug Administration
Published: 1993-02-05

Substantially Equivalent

Specialty Medical Sales, Inc.

FDA 510(k) clearance K921450 for NON-INVASIVE TUBING, Substantially Equivalent on 1993-02-05. Applicant: Specialty Medical Sales, Inc.. Device class: 2.

Clearance details

Applicant: Specialty Medical Sales, Inc.
Product code: Code FPK
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 1992-03-26
Decision date: 1993-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salem, NH, US

Download summary PDF View on FDA.gov ↗

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