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FDA 510(k)

BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER

K-Number: K993292 · 2000-03-23

ApplicantBoston Scientific, Target
Decision Date2000-03-23
Product CodeMJN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific, Target. It received FDA 510(k) clearance on 2000-03-23 under 510(k) number K993292. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER?

BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 2000-03-23. The listed applicant is Boston Scientific, Target. The 510(k) number is K993292.

When did BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER receive FDA 510(k) clearance?

BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER received FDA 510(k) clearance on 2000-03-23, under 510(k) number K993292.

Who is the listed applicant for BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER?

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

What is the FDA product code for BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER?

The FDA product code for BOSTON SCIENTIFIC/TARGET SENTRY OCCLUSION BALLOON CATHETER is MJN.

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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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