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FDA 510(k)

ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE

K-Number: K962584 · 1996-11-04

ApplicantEthicon Endo-Surgery, Inc.
Decision Date1996-11-04
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 1996-11-04 under 510(k) number K962584. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE?

ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE is a medical device that received FDA 510(k) clearance on 1996-11-04. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K962584.

When did ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE receive FDA 510(k) clearance?

ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE received FDA 510(k) clearance on 1996-11-04, under 510(k) number K962584.

Who is the listed applicant for ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE?

The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE?

The FDA product code for ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE is LFL.

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Other records listing Ethicon Endo-Surgery, 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.

K111195VALUTRUS REUSABLE CIRCULAR STAPLER AND DISPOSABLE RELOADSK110385ECHELON FLEX 45 / 60 POWERED ARTICULATING ENDOSCOPIC LINEAR CUTTERK101520ENSEAL TISSUE SEALING DEVICES MODEL: NSEAL514H-535H, NSEAL514RH-535RHK102632ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLERK093896ETHICON ENDO SURGERY SLOTTED ANOSCOPEK091259ETHICON ENDO-SURGERY FLEXIBLE BIPOLAR HEMOSTASIS FORCEPS

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Related Devices (Code: LFL)

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.

K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLCK251162CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences CorporationK242894SanAgile™ Ultrasonic Surgery Advanced Portable Controller (SA10); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD14); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD23); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD36); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD45)Shanghai Saints Sages Surgical Co., Ltd.K243930Sonopet iQ Ultrasonic Aspirator System (5500-050-000)Stryker InstrumentsK241700Tenex 2nd Generation SystemTrice Medical, Inc.K240493CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation

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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