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FDA 510(k)

CONSTELLATION CATHETERS, MODEL 8031M

K-Number: K021232 · 2002-05-16

ApplicantBoston Scientific Corp
Decision Date2002-05-16
Product CodeMTD
Advisory CommitteeCV
DecisionUnknown

Device Summary

CONSTELLATION CATHETERS, MODEL 8031M is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2002-05-16 under 510(k) number K021232. The device is classified under product code MTD. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CONSTELLATION CATHETERS, MODEL 8031M?

CONSTELLATION CATHETERS, MODEL 8031M is a medical device that received FDA 510(k) clearance on 2002-05-16. The listed applicant is Boston Scientific Corp. The 510(k) number is K021232.

When did CONSTELLATION CATHETERS, MODEL 8031M receive FDA 510(k) clearance?

CONSTELLATION CATHETERS, MODEL 8031M received FDA 510(k) clearance on 2002-05-16, under 510(k) number K021232.

Who is the listed applicant for CONSTELLATION CATHETERS, MODEL 8031M?

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

What is the FDA product code for CONSTELLATION CATHETERS, MODEL 8031M?

The FDA product code for CONSTELLATION CATHETERS, MODEL 8031M is MTD.

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Related Devices (Code: MTD)

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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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