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FDA 510(k)

TEFLON CANNULA

K-Number: K822776 · 1982-11-03

ApplicantCardiac Pacemakers, Inc.
Decision Date1982-11-03
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEFLON CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Pacemakers, Inc.. It received FDA 510(k) clearance on 1982-11-03 under 510(k) number K822776. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEFLON CANNULA?

TEFLON CANNULA is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is Cardiac Pacemakers, Inc.. The 510(k) number is K822776.

When did TEFLON CANNULA receive FDA 510(k) clearance?

TEFLON CANNULA received FDA 510(k) clearance on 1982-11-03, under 510(k) number K822776.

Who is the listed applicant for TEFLON CANNULA?

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

What is the FDA product code for TEFLON CANNULA?

The FDA product code for TEFLON CANNULA is FOZ.

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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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