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FDA 510(k)

TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE

K-Number: K905756 · 1991-01-08

ApplicantTitan Technology Intl., Inc.
Decision Date1991-01-08
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Titan Technology Intl., Inc.. It received FDA 510(k) clearance on 1991-01-08 under 510(k) number K905756. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE?

TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE is a medical device that received FDA 510(k) clearance on 1991-01-08. The listed applicant is Titan Technology Intl., Inc.. The 510(k) number is K905756.

When did TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE receive FDA 510(k) clearance?

TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE received FDA 510(k) clearance on 1991-01-08, under 510(k) number K905756.

Who is the listed applicant for TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE?

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

What is the FDA product code for TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE?

The FDA product code for TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE is JFB.

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Related Devices (Code: JFB)

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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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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