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FDA 510(k)

NAGASHIMA KN-52 SACCADE & PURSUIT STIM

K-Number: K822266 · 1982-08-16

ApplicantKelleher Corp.
Decision Date1982-08-16
Product CodeGWN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NAGASHIMA KN-52 SACCADE & PURSUIT STIM is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-16 under 510(k) number K822266. 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 KN-52 SACCADE & PURSUIT STIM?

NAGASHIMA KN-52 SACCADE & PURSUIT STIM is a medical device that received FDA 510(k) clearance on 1982-08-16. The listed applicant is Kelleher Corp.. The 510(k) number is K822266.

When did NAGASHIMA KN-52 SACCADE & PURSUIT STIM receive FDA 510(k) clearance?

NAGASHIMA KN-52 SACCADE & PURSUIT STIM received FDA 510(k) clearance on 1982-08-16, under 510(k) number K822266.

Who is the listed applicant for NAGASHIMA KN-52 SACCADE & PURSUIT STIM?

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 KN-52 SACCADE & PURSUIT STIM?

The FDA product code for NAGASHIMA KN-52 SACCADE & PURSUIT STIM 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 SETK822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPHK823083ELECTROSURGICAL UNITK822252ENT TREATMENT UNITSK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS

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Related Devices (Code: GWN)

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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