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FDA 510(k)

M.D.I. ADAPTER

K-Number: K895549 · 1989-11-21

Decision Date1989-11-21
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

M.D.I. ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Custom Connection Corp.. It received FDA 510(k) clearance on 1989-11-21 under 510(k) number K895549. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.D.I. ADAPTER?

M.D.I. ADAPTER is a medical device that received FDA 510(k) clearance on 1989-11-21. The listed applicant is Custom Connection Corp.. The 510(k) number is K895549.

When did M.D.I. ADAPTER receive FDA 510(k) clearance?

M.D.I. ADAPTER received FDA 510(k) clearance on 1989-11-21, under 510(k) number K895549.

Who is the listed applicant for M.D.I. ADAPTER?

The FDA 510(k) record lists Custom Connection Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M.D.I. ADAPTER?

The FDA product code for M.D.I. ADAPTER is BZA.

Related Clinical Trials

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.

Related Devices (Code: BZA)

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.

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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