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FDA 510(k)

CROSS-CHECKS EO GAS STERILIZATION MONITOR

K-Number: K952244 · 1996-08-05

ApplicantSteritec Products Mfg Co, Inc.
Decision Date1996-08-05
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CROSS-CHECKS EO GAS STERILIZATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Steritec Products Mfg Co, Inc.. It received FDA 510(k) clearance on 1996-08-05 under 510(k) number K952244. 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 CROSS-CHECKS EO GAS STERILIZATION MONITOR?

CROSS-CHECKS EO GAS STERILIZATION MONITOR is a medical device that received FDA 510(k) clearance on 1996-08-05. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K952244.

When did CROSS-CHECKS EO GAS STERILIZATION MONITOR receive FDA 510(k) clearance?

CROSS-CHECKS EO GAS STERILIZATION MONITOR received FDA 510(k) clearance on 1996-08-05, under 510(k) number K952244.

Who is the listed applicant for CROSS-CHECKS EO GAS STERILIZATION MONITOR?

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

What is the FDA product code for CROSS-CHECKS EO GAS STERILIZATION MONITOR?

The FDA product code for CROSS-CHECKS EO GAS STERILIZATION MONITOR is JOJ.

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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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