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FDA 510(k)

MIDMARK M9 ULTRACLAVE STEAM STERILIZER

K-Number: K023348 · 2003-03-03

ApplicantMidmark Corp.
Decision Date2003-03-03
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIDMARK M9 ULTRACLAVE STEAM STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 2003-03-03 under 510(k) number K023348. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDMARK M9 ULTRACLAVE STEAM STERILIZER?

MIDMARK M9 ULTRACLAVE STEAM STERILIZER is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Midmark Corp.. The 510(k) number is K023348.

When did MIDMARK M9 ULTRACLAVE STEAM STERILIZER receive FDA 510(k) clearance?

MIDMARK M9 ULTRACLAVE STEAM STERILIZER received FDA 510(k) clearance on 2003-03-03, under 510(k) number K023348.

Who is the listed applicant for MIDMARK M9 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 M9 ULTRACLAVE STEAM STERILIZER?

The FDA product code for MIDMARK M9 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.

View all 31 devices →

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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