M.D.I. ADAPTER
K-Number: K895549 · 1989-11-21
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Device Summary
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
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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