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FDA 510(k)

BURBANK TENACULUM

K-Number: K060573 · 2006-04-21

ApplicantVascular Control Systems, Inc.
Decision Date2006-04-21
Product CodeHDC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BURBANK TENACULUM is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Control Systems, Inc.. It received FDA 510(k) clearance on 2006-04-21 under 510(k) number K060573. 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 BURBANK TENACULUM?

BURBANK TENACULUM is a medical device that received FDA 510(k) clearance on 2006-04-21. The listed applicant is Vascular Control Systems, Inc.. The 510(k) number is K060573.

When did BURBANK TENACULUM receive FDA 510(k) clearance?

BURBANK TENACULUM received FDA 510(k) clearance on 2006-04-21, under 510(k) number K060573.

Who is the listed applicant for BURBANK TENACULUM?

The FDA 510(k) record lists Vascular Control Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BURBANK TENACULUM?

The FDA product code for BURBANK TENACULUM 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 Vascular Control Systems, Inc. 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.

K052209VCS DOPPLER TRANSCEIVER, MODEL 09-0023-01K032125CSTAT, MODELS 09-0014-01 AND 09-0014-02K031812TRANSVAGINAL DOPPLER CLAMP, MODELS: 09-0016-01, 09-0016-02, 09-0016-03K031358TRANSVAGINAL DOPPLER PROBEK030078BURBANK TENACULUM, MODEL 09-0011-01K023154VCS-A SERIES CLAMP WITH DOPPLER ULTRASOUND, MODEL 09-0007-01 AND 09-0007-02

View all 9 devices →

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, LLCK032585TRANSVAGINAL ULTRASOUND PROBE HOLDER SYSTEMRon-Tech Medical , Ltd.

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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