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FDA 510(k)

NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH

K-Number: K822268 · 1983-01-28

ApplicantKelleher Corp.
Decision Date1983-01-28
Product CodeGWN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1983-01-28 under 510(k) number K822268. The device is classified under product code GWN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH?

NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Kelleher Corp.. The 510(k) number is K822268.

When did NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH receive FDA 510(k) clearance?

NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH received FDA 510(k) clearance on 1983-01-28, under 510(k) number K822268.

Who is the listed applicant for NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH?

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

What is the FDA product code for NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH?

The FDA product code for NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH is GWN.

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Other records listing Kelleher Corp. 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.

K822618EMERGENCY TRACHEOSTOMY INSTRUMENT SETK823083ELECTROSURGICAL UNITK822252ENT TREATMENT UNITSK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDSK822017TYMPANOSTOMY TUBES & VARIOUS TYPES

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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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