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FDA 510(k)

FLEXIBLE FIBERSCOPES AND ACCESSORIES

K-Number: K980401 · 1998-05-21

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1998-05-21
Product CodeFAJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE FIBERSCOPES AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1998-05-21 under 510(k) number K980401. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE FIBERSCOPES AND ACCESSORIES?

FLEXIBLE FIBERSCOPES AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1998-05-21. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K980401.

When did FLEXIBLE FIBERSCOPES AND ACCESSORIES receive FDA 510(k) clearance?

FLEXIBLE FIBERSCOPES AND ACCESSORIES received FDA 510(k) clearance on 1998-05-21, under 510(k) number K980401.

Who is the listed applicant for FLEXIBLE FIBERSCOPES AND ACCESSORIES?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEXIBLE FIBERSCOPES AND ACCESSORIES?

The FDA product code for FLEXIBLE FIBERSCOPES AND ACCESSORIES is FAJ.

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Related Devices (Code: FAJ)

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.

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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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