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FDA 510(k)

A.C.I. TRACH TIE

K-Number: K882891 · 1988-09-19

ApplicantAuxiliary Care, Inc.
Decision Date1988-09-19
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

A.C.I. TRACH TIE is the device name listed in this FDA 510(k) record. The listed applicant is Auxiliary Care, Inc.. It received FDA 510(k) clearance on 1988-09-19 under 510(k) number K882891. 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 A.C.I. TRACH TIE?

A.C.I. TRACH TIE is a medical device that received FDA 510(k) clearance on 1988-09-19. The listed applicant is Auxiliary Care, Inc.. The 510(k) number is K882891.

When did A.C.I. TRACH TIE receive FDA 510(k) clearance?

A.C.I. TRACH TIE received FDA 510(k) clearance on 1988-09-19, under 510(k) number K882891.

Who is the listed applicant for A.C.I. TRACH TIE?

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

What is the FDA product code for A.C.I. TRACH TIE?

The FDA product code for A.C.I. TRACH TIE 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.

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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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