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FDA 510(k)

PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)

K-Number: K031152 · 2004-08-17

Decision Date2004-08-17
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST) is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 2004-08-17 under 510(k) number K031152. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)?

PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST) is a medical device that received FDA 510(k) clearance on 2004-08-17. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K031152.

When did PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST) receive FDA 510(k) clearance?

PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST) received FDA 510(k) clearance on 2004-08-17, under 510(k) number K031152.

Who is the listed applicant for PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)?

The FDA 510(k) record lists Propper Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)?

The FDA product code for PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST) is JOJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Propper Mfg. Co., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 25 devices →

Related Devices (Code: JOJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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