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FDA 510(k)

THE LEWIS TUBE HOLDER

K-Number: K920691 · 1992-03-18

ApplicantR. Lewis, Inc.
Decision Date1992-03-18
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE LEWIS TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is R. Lewis, Inc.. It received FDA 510(k) clearance on 1992-03-18 under 510(k) number K920691. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE LEWIS TUBE HOLDER?

THE LEWIS TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is R. Lewis, Inc.. The 510(k) number is K920691.

When did THE LEWIS TUBE HOLDER receive FDA 510(k) clearance?

THE LEWIS TUBE HOLDER received FDA 510(k) clearance on 1992-03-18, under 510(k) number K920691.

Who is the listed applicant for THE LEWIS TUBE HOLDER?

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

What is the FDA product code for THE LEWIS TUBE HOLDER?

The FDA product code for THE LEWIS TUBE HOLDER is CBH.

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Related Devices (Code: CBH)

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.

K964399DALE ENDOTRACHEAL TUBE HOLDER 270/280Dale Medical Products, Inc.K942529HCI TUBE STABILIZERHealth Care Contracts, Inc.K951491DALE TRACHEOSTOMY TUBE HOLDER WITH TRACH MASK ATTACHMENT TABSDale Medical Products, Inc.K950930TRACHE-TITEThe Varner Group, Inc.K950318FLEX BLUEKing Systems Corp.K942395ENDOTRACHEAL TUBE HOLDERS.T.I. Medical Products Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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