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FDA 510(k)

FLEXIBLE MINI-FIBERSCOPES

K-Number: K962172 · 1996-12-02

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1996-12-02
Product CodeFBN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE MINI-FIBERSCOPES 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 1996-12-02 under 510(k) number K962172. The device is classified under product code FBN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE MINI-FIBERSCOPES?

FLEXIBLE MINI-FIBERSCOPES is a medical device that received FDA 510(k) clearance on 1996-12-02. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K962172.

When did FLEXIBLE MINI-FIBERSCOPES receive FDA 510(k) clearance?

FLEXIBLE MINI-FIBERSCOPES received FDA 510(k) clearance on 1996-12-02, under 510(k) number K962172.

Who is the listed applicant for FLEXIBLE MINI-FIBERSCOPES?

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 MINI-FIBERSCOPES?

The FDA product code for FLEXIBLE MINI-FIBERSCOPES is FBN.

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Related Devices (Code: FBN)

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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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