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FDA 510(k)

TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE

K-Number: K992071 · 1999-08-27

ApplicantRon-Tech Medical , Ltd.
Decision Date1999-08-27
Product CodeHDC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Ron-Tech Medical , Ltd.. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K992071. 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 TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE?

TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Ron-Tech Medical , Ltd.. The 510(k) number is K992071.

When did TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE receive FDA 510(k) clearance?

TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE received FDA 510(k) clearance on 1999-08-27, under 510(k) number K992071.

Who is the listed applicant for TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE?

The FDA 510(k) record lists Ron-Tech Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE?

The FDA product code for TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE is HDC.

Related Clinical Trials

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.

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Other records listing Ron-Tech Medical , Ltd. 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.

K032585TRANSVAGINAL ULTRASOUND PROBE HOLDER SYSTEM

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

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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