FDA 510(k)

THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D

K-Number: K925373 · 1993-05-06

Decision Date1993-05-06

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D is the device name listed in this FDA 510(k) record. The listed applicant is Therex Corp.. It received FDA 510(k) clearance on 1993-05-06 under 510(k) number K925373. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D?

THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D is a medical device that received FDA 510(k) clearance on 1993-05-06. The listed applicant is Therex Corp.. The 510(k) number is K925373.

When did THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D receive FDA 510(k) clearance?

THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D received FDA 510(k) clearance on 1993-05-06, under 510(k) number K925373.

Who is the listed applicant for THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D?

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

What is the FDA product code for THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D?

The FDA product code for THEREX LOW-PROFILE PORT/1.0MM I.D./1.8MM O.D is LJT.

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Other records listing Therex Corp. as applicant

K953110LOW PROFILE TITANIUM MODEL CATALOG #1003 K953017LOW PROFILE TITANIUM MODEL CATALOG #1003 K952537THEREX LOW PROFILE TITANIUM MODEL 1.0MM I.D./1.8MM O.D.K950212A2 DETACHED DUAL PORT SYSTEM K9501311.0MM 1.8MMO.D. POLYURETHANE DETACHED MODEL K942412THEREX LOW-PROFILE PORT - TITANIUM MODEL

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Related Devices (Code: LJT)

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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.