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FDA 510(k)

NAGASHIMA LIGHT SOURCE UNIT SL-4

K-Number: K821708 · 1982-06-25

Decision Date1982-06-25
Product CodeEQN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NAGASHIMA LIGHT SOURCE UNIT SL-4 is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-06-25 under 510(k) number K821708. The device is classified under product code EQN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAGASHIMA LIGHT SOURCE UNIT SL-4?

NAGASHIMA LIGHT SOURCE UNIT SL-4 is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is Kelleher Corp.. The 510(k) number is K821708.

When did NAGASHIMA LIGHT SOURCE UNIT SL-4 receive FDA 510(k) clearance?

NAGASHIMA LIGHT SOURCE UNIT SL-4 received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821708.

Who is the listed applicant for NAGASHIMA LIGHT SOURCE UNIT SL-4?

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 LIGHT SOURCE UNIT SL-4?

The FDA product code for NAGASHIMA LIGHT SOURCE UNIT SL-4 is EQN.

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: EQN)

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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