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FDA 510(k)

ZINC FORMALIN CONCENTRATE

K-Number: K882268 · 1988-06-15

ApplicantAnatech, Ltd.
Decision Date1988-06-15
Product CodeIGG
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

ZINC FORMALIN CONCENTRATE is the device name listed in this FDA 510(k) record. The listed applicant is Anatech, Ltd.. It received FDA 510(k) clearance on 1988-06-15 under 510(k) number K882268. The device is classified under product code IGG. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZINC FORMALIN CONCENTRATE?

ZINC FORMALIN CONCENTRATE is a medical device that received FDA 510(k) clearance on 1988-06-15. The listed applicant is Anatech, Ltd.. The 510(k) number is K882268.

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

ZINC FORMALIN CONCENTRATE received FDA 510(k) clearance on 1988-06-15, under 510(k) number K882268.

Who is the listed applicant for ZINC FORMALIN CONCENTRATE?

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 CONCENTRATE?

The FDA product code for ZINC FORMALIN CONCENTRATE is IGG.

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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 HEMATOXYLINK881282XYLENEK872663DRY-FORMK872498HARRIS HEMATOXYLINK872499ANATECH HEMATOXYLIN-NORMAL STRENGTH

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Related Devices (Code: IGG)

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.

K861201FORMALDEHYDE SOLUTION, 37%Surgipath Medical Industries, Inc.K81179437% FORMALDEHYDERichard-Allan Medical Ind., Inc.K802506PLEASCENT OR FORMA-SCENTMeridian Diagnostics, Inc.K792707PARA-PAK SAFMeridian Diagnostics, Inc.K792705PARA-PAK FORMALINMeridian Diagnostics, Inc.K771201FORMALIN BUFFER CONCENTRATECentral Labs. Assoc. MD Pathologists

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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