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FDA 510(k)

BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES

K-Number: K982557 · 1998-09-10

ApplicantBard Interventional Products Div.
Decision Date1998-09-10
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES is the device name listed in this FDA 510(k) record. The listed applicant is Bard Interventional Products Div.. It received FDA 510(k) clearance on 1998-09-10 under 510(k) number K982557. 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 BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES?

BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES is a medical device that received FDA 510(k) clearance on 1998-09-10. The listed applicant is Bard Interventional Products Div.. The 510(k) number is K982557.

When did BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES receive FDA 510(k) clearance?

BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES received FDA 510(k) clearance on 1998-09-10, under 510(k) number K982557.

Who is the listed applicant for BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES?

The FDA 510(k) record lists Bard Interventional Products Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES?

The FDA product code for BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES is KNS.

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.

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Other records listing Bard Interventional Products Div. 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.

K963484BARD HIGH FLOW PAPILLOTOME

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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