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FDA 510(k)

ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS

K-Number: K972856 · 1998-02-11

ApplicantRocket Medical Plc
Decision Date1998-02-11
Product CodeKNF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS is the device name listed in this FDA 510(k) record. The listed applicant is Rocket Medical Plc. It received FDA 510(k) clearance on 1998-02-11 under 510(k) number K972856. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS?

ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS is a medical device that received FDA 510(k) clearance on 1998-02-11. The listed applicant is Rocket Medical Plc. The 510(k) number is K972856.

When did ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS receive FDA 510(k) clearance?

ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS received FDA 510(k) clearance on 1998-02-11, under 510(k) number K972856.

Who is the listed applicant for ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS?

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

What is the FDA product code for ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS?

The FDA product code for ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS is KNF.

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Other records listing Rocket Medical Plc 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.

K210509Rocket Platinum Cured CathterK163321Rocket Indwelling Pleural Catheter (IPC) Insertion KitK162457Rocket Indwelling Peritoneal Catheter (IPC) Insertion KitK152105Rocket IPC Insertion Set, Rocket IPC Mini Insertion SetK123033ROCKET IPC INSERTION PACK, ROCKET IPC MINI INSERTION SET, ROCKET IPC DRESSING PACK AND BOTTLE SET, ROCKET IPC DRAINAGE BK052365CERVINEEDLE DISPOSABLE CARTRIDGE SYRINGE

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Related Devices (Code: KNF)

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.

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KGK250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, 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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