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FDA 510(k)

ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP

K-Number: K990456 · 1999-03-25

ApplicantHollister, Inc.
Decision Date1999-03-25
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1999-03-25 under 510(k) number K990456. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP?

ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP is a medical device that received FDA 510(k) clearance on 1999-03-25. The listed applicant is Hollister, Inc.. The 510(k) number is K990456.

When did ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP receive FDA 510(k) clearance?

ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP received FDA 510(k) clearance on 1999-03-25, under 510(k) number K990456.

Who is the listed applicant for ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP?

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

What is the FDA product code for ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP?

The FDA product code for ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP is KPI.

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Related Devices (Code: KPI)

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.

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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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