3M BRAND EAR LOOP FACE MASK, 2000F
K-Number: K910182 · 1991-03-04
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Device Summary
Frequently Asked Questions
What is the 3M BRAND EAR LOOP FACE MASK, 2000F?
3M BRAND EAR LOOP FACE MASK, 2000F is a medical device that received FDA 510(k) clearance on 1991-03-04. The listed applicant is 3M Company. The 510(k) number is K910182.
When did 3M BRAND EAR LOOP FACE MASK, 2000F receive FDA 510(k) clearance?
3M BRAND EAR LOOP FACE MASK, 2000F received FDA 510(k) clearance on 1991-03-04, under 510(k) number K910182.
Who is the listed applicant for 3M BRAND EAR LOOP FACE MASK, 2000F?
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 BRAND EAR LOOP FACE MASK, 2000F?
The FDA product code for 3M BRAND EAR LOOP FACE MASK, 2000F is FXX.
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: FXX)
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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