MODEL PB3300 INTRA-ARTER BLOOD GAS MONIT SYS, MODI— 510(k) K931112

Name: FDA 510(k) clearance K931112
Creator: U.S. Food and Drug Administration
Published: 1993-06-01

Substantially Equivalent

Puritan Bennett Corp.

FDA 510(k) clearance K931112 for MODEL PB3300 INTRA-ARTER BLOOD GAS MONIT SYS, MODI, Substantially Equivalent on 1993-06-01. Applicant: Puritan Bennett Corp.. Device class: 2.

Clearance details

Applicant: Puritan Bennett Corp.
Product code: Code CBZ
Device class: Class 2
Regulation: 21 CFR 868.1170
Advisory panel: Anesthesiology
Date received: 1993-03-04
Decision date: 1993-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, CA, US

Download summary PDF View on FDA.gov ↗

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