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FDA 510(k)

ELECTRIC CORD FOR ENDOSCOPE

K-Number: K822254 · 1982-08-20

ApplicantKelleher Corp.
Decision Date1982-08-20
Product CodeFFZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ELECTRIC CORD FOR ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-20 under 510(k) number K822254. The device is classified under product code FFZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC CORD FOR ENDOSCOPE?

ELECTRIC CORD FOR ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1982-08-20. The listed applicant is Kelleher Corp.. The 510(k) number is K822254.

When did ELECTRIC CORD FOR ENDOSCOPE receive FDA 510(k) clearance?

ELECTRIC CORD FOR ENDOSCOPE received FDA 510(k) clearance on 1982-08-20, under 510(k) number K822254.

Who is the listed applicant for ELECTRIC CORD FOR ENDOSCOPE?

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 ELECTRIC CORD FOR ENDOSCOPE?

The FDA product code for ELECTRIC CORD FOR ENDOSCOPE is FFZ.

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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: FFZ)

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.

K111013ACEMSandhill Scientific, Inc.K782046C-CORDConcept, 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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