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FDA 510(k)

CHROMA ZONE COLOR STAIN

K-Number: K012737 · 2001-09-14

Decision Date2001-09-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHROMA ZONE COLOR STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Kuraray Medical, Inc.. It received FDA 510(k) clearance on 2001-09-14 under 510(k) number K012737. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHROMA ZONE COLOR STAIN?

CHROMA ZONE COLOR STAIN is a medical device that received FDA 510(k) clearance on 2001-09-14. The listed applicant is Kuraray Medical, Inc.. The 510(k) number is K012737.

When did CHROMA ZONE COLOR STAIN receive FDA 510(k) clearance?

CHROMA ZONE COLOR STAIN received FDA 510(k) clearance on 2001-09-14, under 510(k) number K012737.

Who is the listed applicant for CHROMA ZONE COLOR STAIN?

The FDA 510(k) record lists Kuraray Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHROMA ZONE COLOR STAIN?

The FDA product code for CHROMA ZONE COLOR STAIN is EBF.

Related Clinical Trials

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.

Other records listing Kuraray Medical, Inc. as applicant

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.

View all 42 devices →

Related Devices (Code: EBF)

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.

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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