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FDA 510(k)

FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS

K-Number: K822265 · 1982-09-28

ApplicantKelleher Corp.
Decision Date1982-09-28
Product CodeEBA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K822265. The device is classified under product code EBA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS?

FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Kelleher Corp.. The 510(k) number is K822265.

When did FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS receive FDA 510(k) clearance?

FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS received FDA 510(k) clearance on 1982-09-28, under 510(k) number K822265.

Who is the listed applicant for FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS?

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 FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS?

The FDA product code for FIBEROPTIC LIGHT SOURCE W/RELATED ITEMS is EBA.

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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: EBA)

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.

K070287PS SERIES WITH FIBER LIGHT GUIDE AND HEADLIGHT, MODELS PS200, PS250, PS500Photonic Optische Gerate GmbH & CokgK923949SYLVAN DENTAL HEADLIGHT SYSTEMSylvan Medical FiberopticsK893458FIBEROPTIC HEADLIGHT SYSTEMCuda Products Co.K854646VEGA DENTAL OPERATING LIGHTAlpine Dental Equipment Co.K842515SURGICAL HEADLIGHTGood-Lite Co.K842358ISOLIGHTPlanmeca USA, Inc.

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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