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FDA 510(k)

ANGIOSCOPE FOR PULMONARY ARTERY USE

K-Number: K882658 · 1989-01-26

ApplicantWashington Regulatory Services
Decision Date1989-01-26
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIOSCOPE FOR PULMONARY ARTERY USE is the device name listed in this FDA 510(k) record. The listed applicant is Washington Regulatory Services. It received FDA 510(k) clearance on 1989-01-26 under 510(k) number K882658. 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 ANGIOSCOPE FOR PULMONARY ARTERY USE?

ANGIOSCOPE FOR PULMONARY ARTERY USE is a medical device that received FDA 510(k) clearance on 1989-01-26. The listed applicant is Washington Regulatory Services. The 510(k) number is K882658.

When did ANGIOSCOPE FOR PULMONARY ARTERY USE receive FDA 510(k) clearance?

ANGIOSCOPE FOR PULMONARY ARTERY USE received FDA 510(k) clearance on 1989-01-26, under 510(k) number K882658.

Who is the listed applicant for ANGIOSCOPE FOR PULMONARY ARTERY USE?

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

What is the FDA product code for ANGIOSCOPE FOR PULMONARY ARTERY USE?

The FDA product code for ANGIOSCOPE FOR PULMONARY ARTERY USE is DQO.

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Related Devices (Code: DQO)

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Official Source

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