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FDA 510(k)

NAGASHIMA SN-SP UNIT AND CHAIR

K-Number: K822016 · 1982-09-14

Decision Date1982-09-14
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NAGASHIMA SN-SP UNIT AND 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 1982-09-14 under 510(k) number K822016. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAGASHIMA SN-SP UNIT AND CHAIR?

NAGASHIMA SN-SP UNIT AND CHAIR is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Kelleher Corp.. The 510(k) number is K822016.

When did NAGASHIMA SN-SP UNIT AND CHAIR receive FDA 510(k) clearance?

NAGASHIMA SN-SP UNIT AND CHAIR received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822016.

Who is the listed applicant for NAGASHIMA SN-SP UNIT AND 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-SP UNIT AND CHAIR?

The FDA product code for NAGASHIMA SN-SP UNIT AND CHAIR is ETF.

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: ETF)

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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