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FDA 510(k)

FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150

K-Number: K893440 · 1989-07-28

ApplicantWelch Allyn, Inc.
Decision Date1989-07-28
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150 is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 1989-07-28 under 510(k) number K893440. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150?

FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150 is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K893440.

When did FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150 receive FDA 510(k) clearance?

FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150 received FDA 510(k) clearance on 1989-07-28, under 510(k) number K893440.

Who is the listed applicant for FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150?

The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150?

The FDA product code for FLEX SIGMOIDOSCOPE LIGHT SOURCE MODEL #45150 is FFS.

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Other records listing Welch Allyn, Inc. as applicant

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Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, Inc.

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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