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FDA 510(k)

CROSS-CHECKS

K-Number: K951113 · 1996-08-19

ApplicantSteritec Products Mfg Co, Inc.
Decision Date1996-08-19
Product CodeLRT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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 1996-08-19 under 510(k) number K951113. The device is classified under product code LRT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROSS-CHECKS?

CROSS-CHECKS is a medical device that received FDA 510(k) clearance on 1996-08-19. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K951113.

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

CROSS-CHECKS received FDA 510(k) clearance on 1996-08-19, under 510(k) number K951113.

Who is the listed applicant for 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 CROSS-CHECKS?

The FDA product code for CROSS-CHECKS is LRT.

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Related Devices (Code: LRT)

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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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