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FDA 510(k)

VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY

K-Number: K844982 · 1985-01-18

Decision Date1985-01-18
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath of Canada , Ltd.. It received FDA 510(k) clearance on 1985-01-18 under 510(k) number K844982. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY?

VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY is a medical device that received FDA 510(k) clearance on 1985-01-18. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K844982.

When did VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY receive FDA 510(k) clearance?

VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY received FDA 510(k) clearance on 1985-01-18, under 510(k) number K844982.

Who is the listed applicant for VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY?

The FDA 510(k) record lists Vas-Cath of Canada , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY?

The FDA product code for VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY is CAZ.

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.

Other records listing Vas-Cath of Canada , 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.

View all 19 devices →

Related Devices (Code: CAZ)

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.

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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