PRECISION MED PRODUCTS LTD VOLUME VENTILATORS— 510(k) K932712

Name: FDA 510(k) clearance K932712
Creator: U.S. Food and Drug Administration
Published: 1993-07-22

Substantially Equivalent

Precision Med Products, Ltd.

FDA 510(k) clearance K932712 for PRECISION MED PRODUCTS LTD VOLUME VENTILATORS, Substantially Equivalent on 1993-07-22. Applicant: Precision Med Products, Ltd.. Device class: 1.

Clearance details

Applicant: Precision Med Products, Ltd.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1993-06-04
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marrtinsville, IN, US

Download summary PDF View on FDA.gov ↗

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K952011 — PRIMA BREATHING BAGS1995-05-22
K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

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K932708 — PRECISION MED PRODUCTS LTD MAPLESON D CIRCUITS1993-07-23
K932709 — PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM1993-07-23
K932710 — GAS SAMPLING LINES AND CONNECTORS1993-07-23

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