3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12
K-Number: K900108 · 1990-02-21
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Device Summary
Frequently Asked Questions
What is the 3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12?
3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12 is a medical device that received FDA 510(k) clearance on 1990-02-21. The listed applicant is 3M Company. The 510(k) number is K900108.
When did 3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12 receive FDA 510(k) clearance?
3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12 received FDA 510(k) clearance on 1990-02-21, under 510(k) number K900108.
Who is the listed applicant for 3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12?
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 MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12?
The FDA product code for 3M MULTI-ALLER. IGE FASTSCREEN S9 W1,6,9,10,11,12 is DGC.
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: DGC)
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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