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FDA 510(k)

ET/RT PAPILLOTOME

K-Number: K860593 · 1986-07-22

ApplicantHobbs Medical, Inc.
Decision Date1986-07-22
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ET/RT PAPILLOTOME is the device name listed in this FDA 510(k) record. The listed applicant is Hobbs Medical, Inc.. It received FDA 510(k) clearance on 1986-07-22 under 510(k) number K860593. 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 ET/RT PAPILLOTOME?

ET/RT PAPILLOTOME is a medical device that received FDA 510(k) clearance on 1986-07-22. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K860593.

When did ET/RT PAPILLOTOME receive FDA 510(k) clearance?

ET/RT PAPILLOTOME received FDA 510(k) clearance on 1986-07-22, under 510(k) number K860593.

Who is the listed applicant for ET/RT PAPILLOTOME?

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

What is the FDA product code for ET/RT PAPILLOTOME?

The FDA product code for ET/RT PAPILLOTOME is KNS.

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Other records listing Hobbs Medical, 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.

K241874Aspiration Catheter (2189)K182927Pulmonary Cytology BrushK093079TOUCHSOFT COAGULATOR WITH BANANA FITTING, MODEL 4581 AND WITH UNIVERSAL FITTING, MODEL 4581-UK030765HOBBS MISTIFIER SPRAY CATHETERK933354HOBBS MEDICAL CLEANING BRUSHK922396FUJINON FORCEPS -- MODIFICATION

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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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