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FDA 510(k)

FIBER OPTIC LIGHT CABLE

K-Number: K932629 · 1993-11-16

ApplicantStephen Chakoff, Inc.
Decision Date1993-11-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC LIGHT CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Stephen Chakoff, Inc.. It received FDA 510(k) clearance on 1993-11-16 under 510(k) number K932629. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC LIGHT CABLE?

FIBER OPTIC LIGHT CABLE is a medical device that received FDA 510(k) clearance on 1993-11-16. The listed applicant is Stephen Chakoff, Inc.. The 510(k) number is K932629.

When did FIBER OPTIC LIGHT CABLE receive FDA 510(k) clearance?

FIBER OPTIC LIGHT CABLE received FDA 510(k) clearance on 1993-11-16, under 510(k) number K932629.

Who is the listed applicant for FIBER OPTIC LIGHT CABLE?

The FDA 510(k) record lists Stephen Chakoff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBER OPTIC LIGHT CABLE?

The FDA product code for FIBER OPTIC LIGHT CABLE is GCJ.

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Other records listing Stephen Chakoff, Inc. 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.

K940316HYSTERSCOPEK940317SINUSCOPEK950753CHAKOFF ENDOSCOPY (CAMERA TELEVISION ENDOSCOPIC WITHOUT AUDIOK951082CHAKOFF ENDOSCOPY, RIGID ENDOSCOPEK950744CHAKOFF ENDOSCOPY (RIDGID ENDOSCOPE)K950748CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)

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Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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