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FDA 510(k)

HCI TUBE STABILIZER

K-Number: K942529 · 1995-06-14

ApplicantHealth Care Contracts, Inc.
Decision Date1995-06-14
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HCI TUBE STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Health Care Contracts, Inc.. It received FDA 510(k) clearance on 1995-06-14 under 510(k) number K942529. 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 HCI TUBE STABILIZER?

HCI TUBE STABILIZER is a medical device that received FDA 510(k) clearance on 1995-06-14. The listed applicant is Health Care Contracts, Inc.. The 510(k) number is K942529.

When did HCI TUBE STABILIZER receive FDA 510(k) clearance?

HCI TUBE STABILIZER received FDA 510(k) clearance on 1995-06-14, under 510(k) number K942529.

Who is the listed applicant for HCI TUBE STABILIZER?

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

What is the FDA product code for HCI TUBE STABILIZER?

The FDA product code for HCI TUBE STABILIZER 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.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.K934288HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BARNeo-Tech, Inc.

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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