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FDA 510(k)

NAGASHIMA SN AUTOMATIC TREATMENT CHAIR

K-Number: K822013 · 1982-07-28

Decision Date1982-07-28
Product CodeGBB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NAGASHIMA SN AUTOMATIC TREATMENT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-07-28 under 510(k) number K822013. The device is classified under product code GBB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAGASHIMA SN AUTOMATIC TREATMENT CHAIR?

NAGASHIMA SN AUTOMATIC TREATMENT CHAIR is a medical device that received FDA 510(k) clearance on 1982-07-28. The listed applicant is Kelleher Corp.. The 510(k) number is K822013.

When did NAGASHIMA SN AUTOMATIC TREATMENT CHAIR receive FDA 510(k) clearance?

NAGASHIMA SN AUTOMATIC TREATMENT CHAIR received FDA 510(k) clearance on 1982-07-28, under 510(k) number K822013.

Who is the listed applicant for NAGASHIMA SN AUTOMATIC TREATMENT CHAIR?

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 SN AUTOMATIC TREATMENT CHAIR?

The FDA product code for NAGASHIMA SN AUTOMATIC TREATMENT CHAIR is GBB.

Related Clinical Trials

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.

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.

View all 94 devices →

Related Devices (Code: GBB)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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