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FDA 510(k)

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L

K-Number: K003533 · 2001-02-07

ApplicantSteritec Products, Inc.
Decision Date2001-02-07
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L 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 2001-02-07 under 510(k) number K003533. 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 LF, MODEL CI 119/S &CI 119/L?

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L is a medical device that received FDA 510(k) clearance on 2001-02-07. The listed applicant is Steritec Products, Inc.. The 510(k) number is K003533.

When did CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L receive FDA 510(k) clearance?

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L received FDA 510(k) clearance on 2001-02-07, under 510(k) number K003533.

Who is the listed applicant for CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L?

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 LF, MODEL CI 119/S &CI 119/L?

The FDA product code for CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L 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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