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FDA 510(k)

STERITUBE

K-Number: K930072 · 1994-06-17

ApplicantJordco, Inc.
Decision Date1994-06-17
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERITUBE is the device name listed in this FDA 510(k) record. The listed applicant is Jordco, Inc.. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K930072. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERITUBE?

STERITUBE is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Jordco, Inc.. The 510(k) number is K930072.

When did STERITUBE receive FDA 510(k) clearance?

STERITUBE received FDA 510(k) clearance on 1994-06-17, under 510(k) number K930072.

Who is the listed applicant for STERITUBE?

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

What is the FDA product code for STERITUBE?

The FDA product code for STERITUBE is KCT.

Related Clinical Trials

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Other records listing Jordco, 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.

K992484RCNG: ROOT CANAL NEGOTIATING GEL; MODEL RCNG

Related Devices (Code: KCT)

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.

K253988LiteSet TraysNobel Biocare ABK261935Surgical and Prosthetic TraysDentsply Sirona, Inc.K253187SteriBest® Sterilization Tray SystemMastel SurgicalK252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AGK253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, 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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