PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM— 510(k) K932709

Name: FDA 510(k) clearance K932709
Creator: U.S. Food and Drug Administration
Published: 1993-07-23

Substantially Equivalent

Precision Med Products, Ltd.

FDA 510(k) clearance K932709 for PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM, Substantially Equivalent on 1993-07-23. Applicant: Precision Med Products, Ltd.. Device class: 2.

Clearance details

Applicant: Precision Med Products, Ltd.
Product code: Code BZR
Device class: Class 2
Regulation: 21 CFR 868.5330
Advisory panel: Anesthesiology
Date received: 1993-06-04
Decision date: 1993-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marrtinsville, IN, US

Download summary PDF View on FDA.gov ↗

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