STERI-VAC GAS STERILIZER MODEL 5XL
K-Number: K902036 · 1990-07-19
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Device Summary
Frequently Asked Questions
What is the STERI-VAC GAS STERILIZER MODEL 5XL?
STERI-VAC GAS STERILIZER MODEL 5XL is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is 3M Company. The 510(k) number is K902036.
When did STERI-VAC GAS STERILIZER MODEL 5XL receive FDA 510(k) clearance?
STERI-VAC GAS STERILIZER MODEL 5XL received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902036.
Who is the listed applicant for STERI-VAC GAS STERILIZER MODEL 5XL?
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 STERI-VAC GAS STERILIZER MODEL 5XL?
The FDA product code for STERI-VAC GAS STERILIZER MODEL 5XL is FLF.
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: FLF)
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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