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FDA 510(k)

UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET

K-Number: K984418 · 1999-03-11

ApplicantMedrad, Inc.
Decision Date1999-03-11
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1999-03-11 under 510(k) number K984418. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET?

UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET is a medical device that received FDA 510(k) clearance on 1999-03-11. The listed applicant is Medrad, Inc.. The 510(k) number is K984418.

When did UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET receive FDA 510(k) clearance?

UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET received FDA 510(k) clearance on 1999-03-11, under 510(k) number K984418.

Who is the listed applicant for UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET?

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

What is the FDA product code for UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET?

The FDA product code for UNIVERSAL ADJUSTABLE T-RAIL TABLE BRACKET is DXT.

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 Medrad, 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.

View all 104 devices →

Related Devices (Code: DXT)

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

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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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