Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PROVIEW SELF-SEALING STERILIZATION POUCH

K-Number: K893802 · 1990-04-04

ApplicantCottrell, Ltd.
Decision Date1990-04-04
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROVIEW SELF-SEALING STERILIZATION POUCH is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1990-04-04 under 510(k) number K893802. 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 PROVIEW SELF-SEALING STERILIZATION POUCH?

PROVIEW SELF-SEALING STERILIZATION POUCH is a medical device that received FDA 510(k) clearance on 1990-04-04. The listed applicant is Cottrell, Ltd.. The 510(k) number is K893802.

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

PROVIEW SELF-SEALING STERILIZATION POUCH received FDA 510(k) clearance on 1990-04-04, under 510(k) number K893802.

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

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

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

The FDA product code for PROVIEW 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 Cottrell, Ltd. 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.

K972708ENDO-SPOR PLUS / HYPROCIDEK970726VAPOCIDEK960089PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATORK952241PROTOUCH OVERGLOVEK952234BARRIER ALL FILMK932922PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR

View all 9 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑