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FDA 510(k)

ELECTRODE, CUTTING LOOP

K-Number: K760178 · 1976-10-15

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-10-15
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ELECTRODE, CUTTING LOOP is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-10-15 under 510(k) number K760178. 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 ELECTRODE, CUTTING LOOP?

ELECTRODE, CUTTING LOOP is a medical device that received FDA 510(k) clearance on 1976-10-15. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760178.

When did ELECTRODE, CUTTING LOOP receive FDA 510(k) clearance?

ELECTRODE, CUTTING LOOP received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760178.

Who is the listed applicant for ELECTRODE, CUTTING LOOP?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRODE, CUTTING LOOP?

The FDA product code for ELECTRODE, CUTTING LOOP is KNS.

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Other records listing V. Mueller O.V. Baxter Healthcare Corp. as applicant

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K803292FIELD SUCTION DISSECTORK792383KELMAN DIPSTICKK771197NORTON ENDOTRACHEALK771302PFISTER-SCHWARTZ STONE RETRIEVERK770959BOUGIE, FILIFORM, JACKSONK770280CORD, ELECTROSURGICAL-STERILE & DISPOS.

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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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