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FDA 510(k)

STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123

K-Number: K003002 · 2000-12-08

ApplicantSteritec Products, Inc.
Decision Date2000-12-08
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123 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 2000-12-08 under 510(k) number K003002. 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 STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123?

STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123 is a medical device that received FDA 510(k) clearance on 2000-12-08. The listed applicant is Steritec Products, Inc.. The 510(k) number is K003002.

When did STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123 receive FDA 510(k) clearance?

STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123 received FDA 510(k) clearance on 2000-12-08, under 510(k) number K003002.

Who is the listed applicant for STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123?

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 STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123?

The FDA product code for STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123 is JOJ.

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Other records listing Steritec Products, Inc. as applicant

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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.

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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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