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FDA 510(k)

CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION)

K-Number: K953205 · 1996-05-23

ApplicantFisher & Paykel Healthcare, Ltd.
Decision Date1996-05-23
Product CodeKOI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Healthcare, Ltd.. It received FDA 510(k) clearance on 1996-05-23 under 510(k) number K953205. The device is classified under product code KOI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION)?

CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K953205.

When did CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION) receive FDA 510(k) clearance?

CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION) received FDA 510(k) clearance on 1996-05-23, under 510(k) number K953205.

Who is the listed applicant for CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION)?

The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION)?

The FDA product code for CONSTANT CURRENT PERIPHERAL NERVE STIMULATOR NS272 (MODIFICATION) is KOI.

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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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