PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)— 510(k) K031152

Name: FDA 510(k) clearance K031152
Creator: U.S. Food and Drug Administration
Published: 2004-08-17

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K031152 for PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST), Substantially Equivalent on 2004-08-17. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 2003-04-11
Decision date: 2004-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island, NY, US

Download summary PDF View on FDA.gov ↗

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