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FDA 510(k)

FLEXIBLE FIBERSCOPES & ACCESSORIES

K-Number: K990397 · 1999-10-25

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1999-10-25
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE FIBERSCOPES & 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 1999-10-25 under 510(k) number K990397. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE FIBERSCOPES & ACCESSORIES?

FLEXIBLE FIBERSCOPES & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1999-10-25. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K990397.

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

FLEXIBLE FIBERSCOPES & ACCESSORIES received FDA 510(k) clearance on 1999-10-25, under 510(k) number K990397.

Who is the listed applicant for FLEXIBLE FIBERSCOPES & 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 & ACCESSORIES?

The FDA product code for FLEXIBLE FIBERSCOPES & ACCESSORIES is HRX.

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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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