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FDA 510(k)

EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124

K-Number: K002861 · 2000-11-29

Decision Date2000-11-29
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124 is the device name listed in this FDA 510(k) record. The listed applicant is Steritec Products, Inc.. It received FDA 510(k) clearance on 2000-11-29 under 510(k) number K002861. 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 EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124?

EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124 is a medical device that received FDA 510(k) clearance on 2000-11-29. The listed applicant is Steritec Products, Inc.. The 510(k) number is K002861.

When did EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124 receive FDA 510(k) clearance?

EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124 received FDA 510(k) clearance on 2000-11-29, under 510(k) number K002861.

Who is the listed applicant for EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124?

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

What is the FDA product code for EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124?

The FDA product code for EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124 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 Steritec Products, 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 12 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

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

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