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FDA 510(k)

ZINC FORMALIN

K-Number: K882874 · 1988-07-28

ApplicantAnatech, Ltd.
Decision Date1988-07-28
Product CodeLDX
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

ZINC FORMALIN 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 K882874. The device is classified under product code LDX. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZINC FORMALIN?

ZINC FORMALIN 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 K882874.

When did ZINC FORMALIN receive FDA 510(k) clearance?

ZINC FORMALIN received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882874.

Who is the listed applicant for ZINC FORMALIN?

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 ZINC FORMALIN?

The FDA product code for ZINC FORMALIN is LDX.

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.

K882873FIELDTEX HEMATOXYLINK882268ZINC FORMALIN CONCENTRATEK881282XYLENEK872663DRY-FORMK872498HARRIS HEMATOXYLINK872499ANATECH HEMATOXYLIN-NORMAL STRENGTH

View all 14 devices →

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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