3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES
K-Number: K880565 · 1988-03-21
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Device Summary
Frequently Asked Questions
What is the 3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES?
3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is 3M Company. The 510(k) number is K880565.
When did 3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES receive FDA 510(k) clearance?
3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES received FDA 510(k) clearance on 1988-03-21, under 510(k) number K880565.
Who is the listed applicant for 3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES?
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 TRIMATIC M MODULAR SYSTEM AND ACCESSORIES?
The FDA product code for 3M TRIMATIC M MODULAR SYSTEM AND ACCESSORIES is IXW.
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: IXW)
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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