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FDA 510(k)

HISTOLOGY PARAFFIN

K-Number: K862141 · 1986-06-13

ApplicantErie Scientific Co.
Decision Date1986-06-13
Product CodeKEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

HISTOLOGY PARAFFIN is the device name listed in this FDA 510(k) record. The listed applicant is Erie Scientific Co.. It received FDA 510(k) clearance on 1986-06-13 under 510(k) number K862141. The device is classified under product code KEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HISTOLOGY PARAFFIN?

HISTOLOGY PARAFFIN is a medical device that received FDA 510(k) clearance on 1986-06-13. The listed applicant is Erie Scientific Co.. The 510(k) number is K862141.

When did HISTOLOGY PARAFFIN receive FDA 510(k) clearance?

HISTOLOGY PARAFFIN received FDA 510(k) clearance on 1986-06-13, under 510(k) number K862141.

Who is the listed applicant for HISTOLOGY PARAFFIN?

The FDA 510(k) record lists Erie Scientific Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HISTOLOGY PARAFFIN?

The FDA product code for HISTOLOGY PARAFFIN is KEO.

Related Clinical Trials

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Related Devices (Code: KEO)

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.

K893772TISSUE EMBEDDING MEDIUMStephens ScientificK862223MICRO THIN* PARAFFINRichard-Allan Medical Ind., Inc.K861270BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.Surgipath Medical Industries, Inc.K842053PARAPLAST EXTRA TISSUE EMBEDDING MED.Sherwood Medical Co.K833071TECHNICON PARACUTTechnicon Instruments Corp.K831580PARAFFIN INFILTRATION MEDIUMSurgipath Medical Industries, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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