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FDA 510(k)

FIELDTEX HEMATOXYLIN

K-Number: K882873 · 1988-07-28

ApplicantAnatech, Ltd.
Decision Date1988-07-28
Product CodeKQC
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FIELDTEX HEMATOXYLIN is the device name listed in this FDA 510(k) record. The listed applicant is Anatech, Ltd.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882873. The device is classified under product code KQC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIELDTEX HEMATOXYLIN?

FIELDTEX HEMATOXYLIN is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Anatech, Ltd.. The 510(k) number is K882873.

When did FIELDTEX HEMATOXYLIN receive FDA 510(k) clearance?

FIELDTEX HEMATOXYLIN received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882873.

Who is the listed applicant for FIELDTEX HEMATOXYLIN?

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

What is the FDA product code for FIELDTEX HEMATOXYLIN?

The FDA product code for FIELDTEX HEMATOXYLIN is KQC.

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.

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Other records listing Anatech, Ltd. 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.

K882874ZINC FORMALINK882268ZINC FORMALIN CONCENTRATEK881282XYLENEK872663DRY-FORMK872498HARRIS HEMATOXYLINK872499ANATECH HEMATOXYLIN-NORMAL STRENGTH

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Related Devices (Code: KQC)

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.

K852843GENERAL DIAGNOSTICS COAG-A-MATE XCWarner-Lambert Co.K843619RETIC-SETR&D Systems, Inc.K841848RETIC-SETR&D Systems, Inc.K792550PONCEAU S STAIN SETElectrophoresis Corp. of AmericaK792496VOLU-SOL NMB RETICULOCYTE STAINVolu Sol Medical IndustriesK791007STAT DIFF STAINBioscientific

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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