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FDA 510(k)

WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT

K-Number: K951519 · 1995-06-14

ApplicantWells Johnson Co.
Decision Date1995-06-14
Product CodeFWL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WECO ENDOSCOPIC SYSTEM 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 1995-06-14 under 510(k) number K951519. The device is classified under product code FWL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT?

WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT is a medical device that received FDA 510(k) clearance on 1995-06-14. The listed applicant is Wells Johnson Co.. The 510(k) number is K951519.

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

WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT received FDA 510(k) clearance on 1995-06-14, under 510(k) number K951519.

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

The FDA product code for WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT is FWL.

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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 SYSTEMK945877WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT

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Related Devices (Code: FWL)

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.

K883760STORZ MODEL 62 ENT CAMERA SYSTEMStorz Instrument 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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