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FDA 510(k)

BICAP ABLATING FORCEPS BAF-7

K-Number: K884306 · 1989-01-05

ApplicantCircon Acmi
Decision Date1989-01-05
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BICAP ABLATING FORCEPS BAF-7 is the device name listed in this FDA 510(k) record. The listed applicant is Circon Acmi. It received FDA 510(k) clearance on 1989-01-05 under 510(k) number K884306. 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 BICAP ABLATING FORCEPS BAF-7?

BICAP ABLATING FORCEPS BAF-7 is a medical device that received FDA 510(k) clearance on 1989-01-05. The listed applicant is Circon Acmi. The 510(k) number is K884306.

When did BICAP ABLATING FORCEPS BAF-7 receive FDA 510(k) clearance?

BICAP ABLATING FORCEPS BAF-7 received FDA 510(k) clearance on 1989-01-05, under 510(k) number K884306.

Who is the listed applicant for BICAP ABLATING FORCEPS BAF-7?

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

What is the FDA product code for BICAP ABLATING FORCEPS BAF-7?

The FDA product code for BICAP ABLATING FORCEPS BAF-7 is KNS.

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Other records listing Circon Acmi 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.

K013165USA SERIES LAPAROSCOPESK980492AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)K905705LAP 3501 HIGH FLOW INSUFFLATORK905706GYN-1500 HYSTEROSCOPIC INUFFLATORK884097MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPESK884025CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200

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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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