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FDA 510(k)

TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS

K-Number: K940203 · 1994-03-30

ApplicantLife-Tech Intl., Inc.
Decision Date1994-03-30
Product CodeFEN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS 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 1994-03-30 under 510(k) number K940203. The device is classified under product code FEN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS?

TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS is a medical device that received FDA 510(k) clearance on 1994-03-30. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K940203.

When did TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS receive FDA 510(k) clearance?

TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS received FDA 510(k) clearance on 1994-03-30, under 510(k) number K940203.

Who is the listed applicant for TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS?

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 TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS?

The FDA product code for TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS is FEN.

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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.

K001129PROLONG, MODELS PL50, PL100, PL150K955031MAXISTIMK954505EZ STIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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Related Devices (Code: FEN)

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.

K212830CT3000ProSrs MedicalK082701URONIRS, MODEL 2000Urodynamix Technologies, Ltd.K073552LABORIE URODYNAMIC SYSTEM WITH TETRA ACCESSORYLaborie Medical Technologies, Corp.K001386ACCUSET SENSOR, MODEL 2000Pelvicare, Inc.K992715NEURO URODYNAMIC SUITE, MODEL 9032E0101Medtronic Functional Diagnostics A/SK983325IN-PROBE II URODYNAMIC SYSTEMInfluence, Inc.

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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