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FDA 510(k)

RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES

K-Number: K926463 · 1994-10-21

ApplicantMidmark Corp.
Decision Date1994-10-21
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1994-10-21 under 510(k) number K926463. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES?

RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES is a medical device that received FDA 510(k) clearance on 1994-10-21. The listed applicant is Midmark Corp.. The 510(k) number is K926463.

When did RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES receive FDA 510(k) clearance?

RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES received FDA 510(k) clearance on 1994-10-21, under 510(k) number K926463.

Who is the listed applicant for RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES?

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 RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES?

The FDA product code for RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCES is FQO.

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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, V5100CK112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

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Related Devices (Code: FQO)

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.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K971307AMSCO SURGICAL TABLESTERIS Corporation

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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