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FDA 510(k)

GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER

K-Number: K874690 · 1988-02-08

ApplicantMentor Corp.
Decision Date1988-02-08
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1988-02-08 under 510(k) number K874690. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER?

GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER is a medical device that received FDA 510(k) clearance on 1988-02-08. The listed applicant is Mentor Corp.. The 510(k) number is K874690.

When did GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER receive FDA 510(k) clearance?

GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER received FDA 510(k) clearance on 1988-02-08, under 510(k) number K874690.

Who is the listed applicant for GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER?

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

What is the FDA product code for GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER?

The FDA product code for GASTROPLASTY CALIBRATING TUBE & GASTROSTENOMETER is FFX.

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Other records listing Mentor Corp. as applicant

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Related Devices (Code: FFX)

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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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