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FDA 510(k)

REUSABLE/DISPOSABLE AUTOPSY KNIFE SET

K-Number: K863549 · 1986-09-30

ApplicantSurgipath Medical Industries, Inc.
Decision Date1986-09-30
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REUSABLE/DISPOSABLE AUTOPSY KNIFE SET is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1986-09-30 under 510(k) number K863549. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE/DISPOSABLE AUTOPSY KNIFE SET?

REUSABLE/DISPOSABLE AUTOPSY KNIFE SET is a medical device that received FDA 510(k) clearance on 1986-09-30. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K863549.

When did REUSABLE/DISPOSABLE AUTOPSY KNIFE SET receive FDA 510(k) clearance?

REUSABLE/DISPOSABLE AUTOPSY KNIFE SET received FDA 510(k) clearance on 1986-09-30, under 510(k) number K863549.

Who is the listed applicant for REUSABLE/DISPOSABLE AUTOPSY KNIFE SET?

The FDA 510(k) record lists Surgipath Medical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REUSABLE/DISPOSABLE AUTOPSY KNIFE SET?

The FDA product code for REUSABLE/DISPOSABLE AUTOPSY KNIFE SET is EMF.

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 Surgipath Medical Industries, Inc. 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.

K883217SCHIFF REAGENTK881921C-E BRUSHK881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVEK881659TISSUE SECTION ADHESIVEK863616KNIFE MAKERK863548ROTARY MICROTOME

View all 30 devices →

Related Devices (Code: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890217MICROSURGICAL KNIVESKinetic Medical ProductsK890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, 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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