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FDA 510(k)

IN-TIME RETRIEVAL DEVICE

K-Number: K014109 · 2002-03-12

ApplicantBoston Scientific, Target
Decision Date2002-03-12
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IN-TIME RETRIEVAL DEVICE 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 2002-03-12 under 510(k) number K014109. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN-TIME RETRIEVAL DEVICE?

IN-TIME RETRIEVAL DEVICE is a medical device that received FDA 510(k) clearance on 2002-03-12. The listed applicant is Boston Scientific, Target. The 510(k) number is K014109.

When did IN-TIME RETRIEVAL DEVICE receive FDA 510(k) clearance?

IN-TIME RETRIEVAL DEVICE received FDA 510(k) clearance on 2002-03-12, under 510(k) number K014109.

Who is the listed applicant for IN-TIME RETRIEVAL DEVICE?

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 IN-TIME RETRIEVAL DEVICE?

The FDA product code for IN-TIME RETRIEVAL DEVICE is MMX.

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Related Devices (Code: MMX)

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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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