FDA 510(k)

CARDIAC CATHETERIZATION KIT

K-Number: K932141 · 1994-09-22

Decision Date1994-09-22

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CARDIAC CATHETERIZATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1994-09-22 under 510(k) number K932141. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIAC CATHETERIZATION KIT?

CARDIAC CATHETERIZATION KIT is a medical device that received FDA 510(k) clearance on 1994-09-22. The listed applicant is Abbott Laboratories. The 510(k) number is K932141.

When did CARDIAC CATHETERIZATION KIT receive FDA 510(k) clearance?

CARDIAC CATHETERIZATION KIT received FDA 510(k) clearance on 1994-09-22, under 510(k) number K932141.

Who is the listed applicant for CARDIAC CATHETERIZATION KIT?

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

What is the FDA product code for CARDIAC CATHETERIZATION KIT?

The FDA product code for CARDIAC CATHETERIZATION KIT is DQO.

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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.