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FDA 510(k)

VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y

K-Number: K843198 · 1984-10-04

Decision Date1984-10-04
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1984-10-04 under 510(k) number K843198. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y?

VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y is a medical device that received FDA 510(k) clearance on 1984-10-04. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K843198.

When did VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y receive FDA 510(k) clearance?

VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y received FDA 510(k) clearance on 1984-10-04, under 510(k) number K843198.

Who is the listed applicant for VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y?

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

What is the FDA product code for VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y?

The FDA product code for VIDEO URODYNAMICS SYS 1906B-Y & 1906C-Y is FET.

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 Life-Tech Intl., 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 68 devices →

Related Devices (Code: FET)

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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