ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK
K-Number: K890771 · 1989-03-14
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Device Summary
Frequently Asked Questions
What is the ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK?
ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is 3M Company. The 510(k) number is K890771.
When did ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK receive FDA 510(k) clearance?
ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK received FDA 510(k) clearance on 1989-03-14, under 510(k) number K890771.
Who is the listed applicant for ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK?
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 ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK?
The FDA product code for ASEPTEX 1812 SUB-MICRON MOLDED SURGICAL MASK 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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