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FDA 510(k)

REFRAX MOUNTING MEDIUM

K-Number: K842986 · 1984-08-21

ApplicantAnatech, Ltd.
Decision Date1984-08-21
Product CodeLEB
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

REFRAX MOUNTING MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Anatech, Ltd.. It received FDA 510(k) clearance on 1984-08-21 under 510(k) number K842986. The device is classified under product code LEB. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REFRAX MOUNTING MEDIUM?

REFRAX MOUNTING MEDIUM is a medical device that received FDA 510(k) clearance on 1984-08-21. The listed applicant is Anatech, Ltd.. The 510(k) number is K842986.

When did REFRAX MOUNTING MEDIUM receive FDA 510(k) clearance?

REFRAX MOUNTING MEDIUM received FDA 510(k) clearance on 1984-08-21, under 510(k) number K842986.

Who is the listed applicant for REFRAX MOUNTING MEDIUM?

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 REFRAX MOUNTING MEDIUM?

The FDA product code for REFRAX MOUNTING MEDIUM is LEB.

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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 FORMALINK882873FIELDTEX HEMATOXYLINK882268ZINC FORMALIN CONCENTRATEK881282XYLENEK872663DRY-FORMK872498HARRIS HEMATOXYLIN

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Related Devices (Code: LEB)

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.

K821019PHOSPHATE BUFFERED CLYCEROL MOUNTING FLUMicrobiological Research Corp.K812193KOH MOUNTING FLUIDAmerican Scientific ProductsK811799CLEAR-MOUNTRichard-Allan Medical Ind., Inc.K760838LACTO-PHENOL COTTON BLUE MOUNTING FL.I M, Inc.

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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