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FDA 510(k)

CB FORMALIN

K-Number: K842862 · 1984-08-28

ApplicantAnatech, Ltd.
Decision Date1984-08-28
Product CodeIGE
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CB 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 1984-08-28 under 510(k) number K842862. The device is classified under product code IGE. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CB FORMALIN?

CB FORMALIN is a medical device that received FDA 510(k) clearance on 1984-08-28. The listed applicant is Anatech, Ltd.. The 510(k) number is K842862.

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

CB FORMALIN received FDA 510(k) clearance on 1984-08-28, under 510(k) number K842862.

Who is the listed applicant for CB 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 CB FORMALIN?

The FDA product code for CB FORMALIN is IGE.

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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 HEMATOXYLINK882874ZINC FORMALINK882268ZINC FORMALIN CONCENTRATEK881282XYLENEK872663DRY-FORMK872498HARRIS HEMATOXYLIN

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Related Devices (Code: IGE)

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.

K950560SALINE SOLUTINE, STERILEBusse Hospital Disposables, 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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