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FDA 510(k)

POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111

K-Number: K000386 · 2000-05-05

Decision Date2000-05-05
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Functional Diagnostics A/S. It received FDA 510(k) clearance on 2000-05-05 under 510(k) number K000386. 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 POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111?

POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111 is a medical device that received FDA 510(k) clearance on 2000-05-05. The listed applicant is Medtronic Functional Diagnostics A/S. The 510(k) number is K000386.

When did POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111 receive FDA 510(k) clearance?

POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111 received FDA 510(k) clearance on 2000-05-05, under 510(k) number K000386.

Who is the listed applicant for POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111?

The FDA 510(k) record lists Medtronic Functional Diagnostics A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111?

The FDA product code for POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111 is FFX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medtronic Functional Diagnostics A/S as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 11 devices →

Related Devices (Code: FFX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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