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FDA 510(k)

CLEARVISION

K-Number: K112380 · 2011-11-22

ApplicantMidmark Corp.
Decision Date2011-11-22
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEARVISION is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 2011-11-22 under 510(k) number K112380. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARVISION?

CLEARVISION is a medical device that received FDA 510(k) clearance on 2011-11-22. The listed applicant is Midmark Corp.. The 510(k) number is K112380.

When did CLEARVISION receive FDA 510(k) clearance?

CLEARVISION received FDA 510(k) clearance on 2011-11-22, under 510(k) number K112380.

Who is the listed applicant for CLEARVISION?

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 CLEARVISION?

The FDA product code for CLEARVISION is MUH.

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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.

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZERK990189MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZER

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Related Devices (Code: MUH)

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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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