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FDA 510(k)

CROSSTEX SELF-SEALING STERILIZATION POUCH

K-Number: K941327 · 1994-12-22

ApplicantCross Country Paper Products Corp.
Decision Date1994-12-22
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CROSSTEX SELF-SEALING STERILIZATION POUCH is the device name listed in this FDA 510(k) record. The listed applicant is Cross Country Paper Products Corp.. It received FDA 510(k) clearance on 1994-12-22 under 510(k) number K941327. 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 CROSSTEX SELF-SEALING STERILIZATION POUCH?

CROSSTEX SELF-SEALING STERILIZATION POUCH is a medical device that received FDA 510(k) clearance on 1994-12-22. The listed applicant is Cross Country Paper Products Corp.. The 510(k) number is K941327.

When did CROSSTEX SELF-SEALING STERILIZATION POUCH receive FDA 510(k) clearance?

CROSSTEX SELF-SEALING STERILIZATION POUCH received FDA 510(k) clearance on 1994-12-22, under 510(k) number K941327.

Who is the listed applicant for CROSSTEX SELF-SEALING STERILIZATION POUCH?

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

What is the FDA product code for CROSSTEX SELF-SEALING STERILIZATION POUCH?

The FDA product code for CROSSTEX SELF-SEALING STERILIZATION POUCH is KCT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cross Country Paper Products Corp. 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.

K861727COTTON FILLED GAUZE SPONGES 2 X 2K844759SURGICAL SCALPEL BLADES & DISPOSABLES

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 SurgicalK260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AGK252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, Inc.

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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