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FDA 510(k)

CAP PORP, CAP TORP

K-Number: K000256 · 2000-02-11

ApplicantGyrus Ent LLC
Decision Date2000-02-11
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CAP PORP, CAP TORP is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Ent LLC. It received FDA 510(k) clearance on 2000-02-11 under 510(k) number K000256. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP PORP, CAP TORP?

CAP PORP, CAP TORP is a medical device that received FDA 510(k) clearance on 2000-02-11. The listed applicant is Gyrus Ent LLC. The 510(k) number is K000256.

When did CAP PORP, CAP TORP receive FDA 510(k) clearance?

CAP PORP, CAP TORP received FDA 510(k) clearance on 2000-02-11, under 510(k) number K000256.

Who is the listed applicant for CAP PORP, CAP TORP?

The FDA 510(k) record lists Gyrus Ent LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAP PORP, CAP TORP?

The FDA product code for CAP PORP, CAP TORP is ETB.

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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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