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FDA 510(k)

TISSUE EMBEDDING MEDIUM

K-Number: K893772 · 1989-06-22

ApplicantStephens Scientific
Decision Date1989-06-22
Product CodeKEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

TISSUE EMBEDDING MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Stephens Scientific. It received FDA 510(k) clearance on 1989-06-22 under 510(k) number K893772. 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 TISSUE EMBEDDING MEDIUM?

TISSUE EMBEDDING MEDIUM is a medical device that received FDA 510(k) clearance on 1989-06-22. The listed applicant is Stephens Scientific. The 510(k) number is K893772.

When did TISSUE EMBEDDING MEDIUM receive FDA 510(k) clearance?

TISSUE EMBEDDING MEDIUM received FDA 510(k) clearance on 1989-06-22, under 510(k) number K893772.

Who is the listed applicant for TISSUE EMBEDDING MEDIUM?

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

What is the FDA product code for TISSUE EMBEDDING MEDIUM?

The FDA product code for TISSUE EMBEDDING MEDIUM is KEO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stephens Scientific 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.

K881359DECALCIFYING SOLUTION IIK872625DECALCIFYING SOLUTIONK832011AMERI CLEAR

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.

K862223MICRO THIN* PARAFFINRichard-Allan Medical Ind., Inc.K862141HISTOLOGY PARAFFINErie Scientific Co.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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