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FDA 510(k)

RIGID CULDOSCOPE AND ACCESSORIES

K-Number: K980972 · 1998-06-12

ApplicantCircon Corp.
Decision Date1998-06-12
Product CodeHEW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RIGID CULDOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Circon Corp.. It received FDA 510(k) clearance on 1998-06-12 under 510(k) number K980972. The device is classified under product code HEW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIGID CULDOSCOPE AND ACCESSORIES?

RIGID CULDOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1998-06-12. The listed applicant is Circon Corp.. The 510(k) number is K980972.

When did RIGID CULDOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

RIGID CULDOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1998-06-12, under 510(k) number K980972.

Who is the listed applicant for RIGID CULDOSCOPE AND ACCESSORIES?

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

What is the FDA product code for RIGID CULDOSCOPE AND ACCESSORIES?

The FDA product code for RIGID CULDOSCOPE AND ACCESSORIES is HEW.

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Other records listing Circon Corp. 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.

K992544TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEMK992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMK981611SNAP-N-PEEL INTRODUCERSK973820USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODEK964594VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)

Related Devices (Code: HEW)

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.

K243152GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access DeviceApplied Medical Resources Corp.K201086Advincula Delineator Uterine ManipulatorCooperSurgical, Inc.K191294Transvaginal Access PlatformApplied Medical Resources Corp.K180429Advincula Delineator Uterine ManipulatorCooperSurgical, Inc.K161065ColpoWave™ Colpotomizer and CerviGrip™ Uterine ManipulatorSurgitools Pty , Ltd.K111014LSI SOLUTIONS FORNISEE SYSTEM UTERINE MANIPULATOR AND ACCESSORIESLsi Solutions, Inc.

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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