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FDA 510(k)

AESCULAP THORACOSCOPIC INSTRUMENTS

K-Number: K944955 · 1994-11-09

ApplicantAesculap, Inc.
Decision Date1994-11-09
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AESCULAP THORACOSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1994-11-09 under 510(k) number K944955. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP THORACOSCOPIC INSTRUMENTS?

AESCULAP THORACOSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-11-09. The listed applicant is Aesculap, Inc.. The 510(k) number is K944955.

When did AESCULAP THORACOSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

AESCULAP THORACOSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1994-11-09, under 510(k) number K944955.

Who is the listed applicant for AESCULAP THORACOSCOPIC INSTRUMENTS?

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

What is the FDA product code for AESCULAP THORACOSCOPIC INSTRUMENTS?

The FDA product code for AESCULAP THORACOSCOPIC INSTRUMENTS is KNS.

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Other records listing Aesculap, 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.

K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

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Related Devices (Code: KNS)

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.

K262460Rezum SystemBoston ScientificK260962SphincterotomeTaewoong Medical Co., Ltd.K252388Vanquish Water Vapor Ablation DeviceFrancis Medical, Inc.K252889Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)Olympus Medical Systems CorporationK250945Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)Olympus Medical Systems Corp.K250351Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U)Olympus Medical Systems 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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