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FDA 510(k)

MODIFIED POLYCHROME IV STAIN

K-Number: K894045 · 1989-07-25

ApplicantDevetec, Inc.
Decision Date1989-07-25
Product CodeKFD
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MODIFIED POLYCHROME IV STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Devetec, Inc.. It received FDA 510(k) clearance on 1989-07-25 under 510(k) number K894045. The device is classified under product code KFD. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED POLYCHROME IV STAIN?

MODIFIED POLYCHROME IV STAIN is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is Devetec, Inc.. The 510(k) number is K894045.

When did MODIFIED POLYCHROME IV STAIN receive FDA 510(k) clearance?

MODIFIED POLYCHROME IV STAIN received FDA 510(k) clearance on 1989-07-25, under 510(k) number K894045.

Who is the listed applicant for MODIFIED POLYCHROME IV STAIN?

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

What is the FDA product code for MODIFIED POLYCHROME IV STAIN?

The FDA product code for MODIFIED POLYCHROME IV STAIN is KFD.

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 Devetec, 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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