FDA 510(k)

STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR

K-Number: K982547 · 1998-10-08

Decision Date1998-10-08

Product CodeJOJ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR 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 1998-10-08 under 510(k) number K982547. 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 STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR?

STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR is a medical device that received FDA 510(k) clearance on 1998-10-08. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K982547.

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

STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR received FDA 510(k) clearance on 1998-10-08, under 510(k) number K982547.

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

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 STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR?

The FDA product code for STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR is 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.