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FDA 510(k)

TBAN

K-Number: K963252 · 1996-09-20

ApplicantBoston Scientific Corp
Decision Date1996-09-20
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TBAN 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 1996-09-20 under 510(k) number K963252. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TBAN?

TBAN is a medical device that received FDA 510(k) clearance on 1996-09-20. The listed applicant is Boston Scientific Corp. The 510(k) number is K963252.

When did TBAN receive FDA 510(k) clearance?

TBAN received FDA 510(k) clearance on 1996-09-20, under 510(k) number K963252.

Who is the listed applicant for TBAN?

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 TBAN?

The FDA product code for TBAN is EOQ.

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Related Devices (Code: EOQ)

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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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