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FDA 510(k)

FIBEROPTIC ILLUMINATED INSTRUMENTS

K-Number: K934269 · 1994-05-17

ApplicantVisitec Co.
Decision Date1994-05-17
Product CodeHJM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FIBEROPTIC ILLUMINATED INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1994-05-17 under 510(k) number K934269. The device is classified under product code HJM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBEROPTIC ILLUMINATED INSTRUMENTS?

FIBEROPTIC ILLUMINATED INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-05-17. The listed applicant is Visitec Co.. The 510(k) number is K934269.

When did FIBEROPTIC ILLUMINATED INSTRUMENTS receive FDA 510(k) clearance?

FIBEROPTIC ILLUMINATED INSTRUMENTS received FDA 510(k) clearance on 1994-05-17, under 510(k) number K934269.

Who is the listed applicant for FIBEROPTIC ILLUMINATED INSTRUMENTS?

The FDA 510(k) record lists Visitec Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBEROPTIC ILLUMINATED INSTRUMENTS?

The FDA product code for FIBEROPTIC ILLUMINATED INSTRUMENTS is HJM.

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Other records listing Visitec Co. 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.

K953394VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}K945114VISITEC SCLERAL PLUGK945738VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEK945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSK942234VISITEC PRECISE-POINTK940210VISITEC EYE PAD

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Related Devices (Code: HJM)

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.

K972506INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATORInfinitech, Inc.K950529PEREGRINE DIFFUSION LIGHT PIPEPeregrine Surgical , Ltd.K945877WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHTWells Johnson Co.K931072HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBEHgm, Inc.K933445DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)Storz Instrument Co.K940393PEREGRINE WIDE ANGLE LIGHT PIPEPeregrine Surgical , Ltd.

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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