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FDA 510(k)

BYRD EXTRACTOR SET

K-Number: K893480 · 1989-06-23

ApplicantMedical Engineering and Development Institute
Decision Date1989-06-23
Product CodeGCC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BYRD EXTRACTOR SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering and Development Institute. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K893480. The device is classified under product code GCC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BYRD EXTRACTOR SET?

BYRD EXTRACTOR SET is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Medical Engineering and Development Institute. The 510(k) number is K893480.

When did BYRD EXTRACTOR SET receive FDA 510(k) clearance?

BYRD EXTRACTOR SET received FDA 510(k) clearance on 1989-06-23, under 510(k) number K893480.

Who is the listed applicant for BYRD EXTRACTOR SET?

The FDA 510(k) record lists Medical Engineering and Development Institute as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BYRD EXTRACTOR SET?

The FDA product code for BYRD EXTRACTOR SET is GCC.

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 Medical Engineering and Development Institute 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.

K902477WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL SETK902469BYRD DILATOR SHEATH SET - TEFLONK902502BYRD STAINLESS STEEL DILATORK895030LIFE-LINE(TM) VASCULAR ACCESS SYSTEMK890820LOCKING WIRE GUIDE STYLET

Related Devices (Code: GCC)

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.

K981061INTRAVASCULAR RETRIEVAL DEVICEMed Institute, Inc.K922354BYRD TELESCOPING STAINLESS STEEL DILAT SHEATH SETMed Institute, Inc.K902502BYRD STAINLESS STEEL DILATORMedical Engineering and Development InstituteK820865VAN-TEC FASCIAL DILATORVan-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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