FDA 510(k)

KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES

K-Number: K944793 · 1995-01-24

ApplicantKARL STORZ Endoscopy-America, Inc.

Decision Date1995-01-24

Product CodeKNF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-01-24 under 510(k) number K944793. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES?

KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K944793.

When did KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES receive FDA 510(k) clearance?

KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES received FDA 510(k) clearance on 1995-01-24, under 510(k) number K944793.

Who is the listed applicant for KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES?

The FDA product code for KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODES is KNF.

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Other records listing KARL STORZ Endoscopy-America, Inc. as applicant

K252624KARL STORZ Laryngoscopes and Accessories K240506KARL STORZ Holders K223885HOPKINS Telescopes K230359KOH Ultramicro Injection Cannula (26167NN); Suction a. Irrig. Cannula,L. 36cm (37360CP); Suction a. Irrig. Cannula,L. 36cm (37360SC); Suction and Irrig Cannula,l. 36cm (37560LH); Suction a. Irrig. Cannula,L. 30cm (37260LH); KOH Ultramicro Injection Needle (26167NA); Puncture Needle, LUER-lock (26178R); Suction a. Irrig. Cannula,L. 43cm (37460LH); Suction a. Irrig. Cannula,L. 36cm (37360LH); Puncture Needle, dia. 1.6 mm, 36 cm (26175R); Two-Way Stopcock (26167H); Injection Needle, LUER-K223520UNIDRIVE SIII System K223923HOPKINS Telescopes

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Related Devices (Code: KNF)

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KG K250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.

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.