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FDA 510(k)

CROSS-CHECKS DUAL, MODEL CI 125

K-Number: K010534 · 2001-08-06

ApplicantSteritec Products, Inc.
Decision Date2001-08-06
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CROSS-CHECKS DUAL, MODEL CI 125 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 2001-08-06 under 510(k) number K010534. 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 DUAL, MODEL CI 125?

CROSS-CHECKS DUAL, MODEL CI 125 is a medical device that received FDA 510(k) clearance on 2001-08-06. The listed applicant is Steritec Products, Inc.. The 510(k) number is K010534.

When did CROSS-CHECKS DUAL, MODEL CI 125 receive FDA 510(k) clearance?

CROSS-CHECKS DUAL, MODEL CI 125 received FDA 510(k) clearance on 2001-08-06, under 510(k) number K010534.

Who is the listed applicant for CROSS-CHECKS DUAL, MODEL CI 125?

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 CROSS-CHECKS DUAL, MODEL CI 125?

The FDA product code for CROSS-CHECKS DUAL, MODEL CI 125 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.

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