3M DIGITAL DISK INTERFACE UNIT
K-Number: K920268 · 1992-05-27
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Device Summary
Frequently Asked Questions
What is the 3M DIGITAL DISK INTERFACE UNIT?
3M DIGITAL DISK INTERFACE UNIT is a medical device that received FDA 510(k) clearance on 1992-05-27. The listed applicant is 3M Company. The 510(k) number is K920268.
When did 3M DIGITAL DISK INTERFACE UNIT receive FDA 510(k) clearance?
3M DIGITAL DISK INTERFACE UNIT received FDA 510(k) clearance on 1992-05-27, under 510(k) number K920268.
Who is the listed applicant for 3M DIGITAL DISK INTERFACE UNIT?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3M DIGITAL DISK INTERFACE UNIT?
The FDA product code for 3M DIGITAL DISK INTERFACE UNIT is LMD.
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.
Other records listing 3M Company as applicant
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: LMD)
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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