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FDA 510(k)

NAMIC PTCA Y-ADAPTOR

K-Number: K900652 · 1990-06-26

ApplicantNorth American Instrument Corp.
Decision Date1990-06-26
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NAMIC PTCA Y-ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K900652. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAMIC PTCA Y-ADAPTOR?

NAMIC PTCA Y-ADAPTOR is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is North American Instrument Corp.. The 510(k) number is K900652.

When did NAMIC PTCA Y-ADAPTOR receive FDA 510(k) clearance?

NAMIC PTCA Y-ADAPTOR received FDA 510(k) clearance on 1990-06-26, under 510(k) number K900652.

Who is the listed applicant for NAMIC PTCA Y-ADAPTOR?

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

What is the FDA product code for NAMIC PTCA Y-ADAPTOR?

The FDA product code for NAMIC PTCA Y-ADAPTOR is DTL.

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Other records listing North American Instrument Corp. as applicant

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Related Devices (Code: DTL)

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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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