FDA 510(k)

CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272

K-Number: K924234 · 1993-05-27

ApplicantFisher & Paykel Electronics , Ltd.

Decision Date1993-05-27

Product CodeKOI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272 is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Electronics , Ltd.. It received FDA 510(k) clearance on 1993-05-27 under 510(k) number K924234. 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 CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272?

CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272 is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is Fisher & Paykel Electronics , Ltd.. The 510(k) number is K924234.

When did CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272 receive FDA 510(k) clearance?

CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272 received FDA 510(k) clearance on 1993-05-27, under 510(k) number K924234.

Who is the listed applicant for CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272?

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

What is the FDA product code for CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272?

The FDA product code for CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272 is KOI.

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Related Devices (Code: 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.