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FDA 510(k)

STERITEC CROSS-CHECKS

K-Number: K955426 · 1996-03-12

ApplicantSteritec Products Mfg Co, Inc.
Decision Date1996-03-12
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERITEC CROSS-CHECKS 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 1996-03-12 under 510(k) number K955426. 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?

STERITEC CROSS-CHECKS is a medical device that received FDA 510(k) clearance on 1996-03-12. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K955426.

When did STERITEC CROSS-CHECKS receive FDA 510(k) clearance?

STERITEC CROSS-CHECKS received FDA 510(k) clearance on 1996-03-12, under 510(k) number K955426.

Who is the listed applicant for STERITEC CROSS-CHECKS?

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?

The FDA product code for STERITEC CROSS-CHECKS is JOJ.

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Other records listing Steritec Products Mfg Co, 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.

K2619923M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)Solventum US, LLCK260181LF Process Indicator Tape for Steam SterilizationIntertape Polymer GroupK251991SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213)Shenzhen Safesecure Medical Infection Control Tech Co. , Ltd.K251035DISINTEK™ PA Test StripsSerim ResearchK251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118STERIS CorporationK243876VERIFY STEAM Integrating IndicatorSTERIS Corporation

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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