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FDA 510(k)

CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS

K-Number: K900814 · 1990-12-17

ApplicantIntellimetrics Instrument Corp.
Decision Date1990-12-17
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Intellimetrics Instrument Corp.. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K900814. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS?

CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is Intellimetrics Instrument Corp.. The 510(k) number is K900814.

When did CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS receive FDA 510(k) clearance?

CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS received FDA 510(k) clearance on 1990-12-17, under 510(k) number K900814.

Who is the listed applicant for CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS?

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

What is the FDA product code for CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS?

The FDA product code for CATH LAB AUTOMATED INTERACTIVE RECORDER SYSTEMS is DQK.

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Related Devices (Code: DQK)

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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.

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