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FDA 510(k)

712 PLASTIC SURGERY TABLE & ACCESORIES

K-Number: K915141 · 1992-01-09

ApplicantMidmark Corp.
Decision Date1992-01-09
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

712 PLASTIC SURGERY TABLE & ACCESORIES is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1992-01-09 under 510(k) number K915141. 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 712 PLASTIC SURGERY TABLE & ACCESORIES?

712 PLASTIC SURGERY TABLE & ACCESORIES is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Midmark Corp.. The 510(k) number is K915141.

When did 712 PLASTIC SURGERY TABLE & ACCESORIES receive FDA 510(k) clearance?

712 PLASTIC SURGERY TABLE & ACCESORIES received FDA 510(k) clearance on 1992-01-09, under 510(k) number K915141.

Who is the listed applicant for 712 PLASTIC SURGERY TABLE & ACCESORIES?

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 712 PLASTIC SURGERY TABLE & ACCESORIES?

The FDA product code for 712 PLASTIC SURGERY TABLE & ACCESORIES 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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