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FDA 510(k)

BRADLEY TENACULUM HOLDER

K-Number: K903649 · 1990-11-02

Decision Date1990-11-02
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRADLEY TENACULUM HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1990-11-02 under 510(k) number K903649. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRADLEY TENACULUM HOLDER?

BRADLEY TENACULUM HOLDER is a medical device that received FDA 510(k) clearance on 1990-11-02. The listed applicant is Marlo Surgical Technology. The 510(k) number is K903649.

When did BRADLEY TENACULUM HOLDER receive FDA 510(k) clearance?

BRADLEY TENACULUM HOLDER received FDA 510(k) clearance on 1990-11-02, under 510(k) number K903649.

Who is the listed applicant for BRADLEY TENACULUM HOLDER?

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

What is the FDA product code for BRADLEY TENACULUM HOLDER?

The FDA product code for BRADLEY TENACULUM HOLDER is KDC.

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.

Other records listing Marlo Surgical Technology 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.

View all 28 devices →

Related Devices (Code: KDC)

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.

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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