MIDMARK M-11 ULTRACLAVE STEAM STERILIZER
K-Number: K936181 · 1994-11-30
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Device Summary
Frequently Asked Questions
What is the MIDMARK M-11 ULTRACLAVE STEAM STERILIZER?
MIDMARK M-11 ULTRACLAVE STEAM STERILIZER is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Midmark Corp.. The 510(k) number is K936181.
When did MIDMARK M-11 ULTRACLAVE STEAM STERILIZER receive FDA 510(k) clearance?
MIDMARK M-11 ULTRACLAVE STEAM STERILIZER received FDA 510(k) clearance on 1994-11-30, under 510(k) number K936181.
Who is the listed applicant for MIDMARK M-11 ULTRACLAVE STEAM STERILIZER?
The FDA 510(k) record lists Midmark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIDMARK M-11 ULTRACLAVE STEAM STERILIZER?
The FDA product code for MIDMARK M-11 ULTRACLAVE STEAM STERILIZER is FLE.
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 Midmark Corp. 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: FLE)
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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