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FDA 510(k)

UTERINE TENACLUM HOOK

K-Number: K001818 · 2000-08-30

ApplicantTowne Brothers (Pvt.), Ltd.
Decision Date2000-08-30
Product CodeHDC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UTERINE TENACLUM HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Towne Brothers (Pvt.), Ltd.. It received FDA 510(k) clearance on 2000-08-30 under 510(k) number K001818. The device is classified under product code HDC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UTERINE TENACLUM HOOK?

UTERINE TENACLUM HOOK is a medical device that received FDA 510(k) clearance on 2000-08-30. The listed applicant is Towne Brothers (Pvt.), Ltd.. The 510(k) number is K001818.

When did UTERINE TENACLUM HOOK receive FDA 510(k) clearance?

UTERINE TENACLUM HOOK received FDA 510(k) clearance on 2000-08-30, under 510(k) number K001818.

Who is the listed applicant for UTERINE TENACLUM HOOK?

The FDA 510(k) record lists Towne Brothers (Pvt.), Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UTERINE TENACLUM HOOK?

The FDA product code for UTERINE TENACLUM HOOK is HDC.

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Related Devices (Code: HDC)

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.

K223866Carevix™ Suction Cervical StabilizerAspivix SAK203820ASPIVIX v1.1 Cervical Suction TenaculumAspivix SAK082349JARIT HULKA UTERINE TENACULUM FORCEPSJ. Jamner Surgical Instruments, Inc.K073182GYN DISPOSABLES TENACULUM 356TGyn-Disposables, Inc.K062563FEMTEN CERVICAL TENACULUMFem Suite, LLCK060573BURBANK TENACULUMVascular Control Systems, 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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