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FDA 510(k)

TUBING EXTENSION SET

K-Number: K993361 · 2000-01-04

ApplicantHurricane Medical
Decision Date2000-01-04
Product CodeMSR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TUBING EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Hurricane Medical. It received FDA 510(k) clearance on 2000-01-04 under 510(k) number K993361. The device is classified under product code MSR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING EXTENSION SET?

TUBING EXTENSION SET is a medical device that received FDA 510(k) clearance on 2000-01-04. The listed applicant is Hurricane Medical. The 510(k) number is K993361.

When did TUBING EXTENSION SET receive FDA 510(k) clearance?

TUBING EXTENSION SET received FDA 510(k) clearance on 2000-01-04, under 510(k) number K993361.

Who is the listed applicant for TUBING EXTENSION SET?

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

What is the FDA product code for TUBING EXTENSION SET?

The FDA product code for TUBING EXTENSION SET is MSR.

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.

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Other records listing Hurricane Medical 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.

K990672LACRIMAL INTUBATION SET, DACRYOCYSTORHINOSTOMY (DCR) SETK990671DRAINAGE WICK; SURGICAL SPEARS AND SPONGES, CORNEAL LIGHT SHIELD, INSTRUMENT WIPE

Related Devices (Code: MSR)

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.

K983448ML UNIVERSAL TUBINGMed-Logics, Inc.K980849SURGIN KITSurgin Surgical Instrumentation, Inc.K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKStorz Instrument Co.K972522ML-DISPOSABLE PAKMed-Logics, 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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