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FDA 510(k)

WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT

K-Number: K945877 · 1995-03-02

ApplicantWells Johnson Co.
Decision Date1995-03-02
Product CodeHJM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Wells Johnson Co.. It received FDA 510(k) clearance on 1995-03-02 under 510(k) number K945877. 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 WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT?

WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT is a medical device that received FDA 510(k) clearance on 1995-03-02. The listed applicant is Wells Johnson Co.. The 510(k) number is K945877.

When did WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT receive FDA 510(k) clearance?

WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT received FDA 510(k) clearance on 1995-03-02, under 510(k) number K945877.

Who is the listed applicant for WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT?

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

What is the FDA product code for WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT?

The FDA product code for WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT is HJM.

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Other records listing Wells Johnson 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.

K991437WELLS JOHNSON INFUSION SYSTEM, MODEL 20-6000-00K984448BIRCOLL BALLOON DISSECTORK971580UAS ULTRASONIC ASPIRATOR SYSTEMK945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTK945500WELLS JOHNSON FIXATION SYSTEMK951519WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT

View all 15 devices →

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.K931072HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBEHgm, Inc.K933445DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)Storz Instrument Co.K940393PEREGRINE WIDE ANGLE LIGHT PIPEPeregrine Surgical , Ltd.K934269FIBEROPTIC ILLUMINATED INSTRUMENTSVisitec Co.

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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