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FDA 510(k)

PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR

K-Number: K973585 · 1998-11-06

ApplicantPropper Mfg. Co., Inc.
Decision Date1998-11-06
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR 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 1998-11-06 under 510(k) number K973585. 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 EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR?

PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR is a medical device that received FDA 510(k) clearance on 1998-11-06. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K973585.

When did PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR receive FDA 510(k) clearance?

PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR received FDA 510(k) clearance on 1998-11-06, under 510(k) number K973585.

Who is the listed applicant for PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR?

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 EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR?

The FDA product code for PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR is JOJ.

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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.

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Related Devices (Code: JOJ)

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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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