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FDA 510(k)

DR7700 OPERATING TABLE

K-Number: K864325 · 1986-11-19

ApplicantKoken Mfg Company, Inc.
Decision Date1986-11-19
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DR7700 OPERATING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Koken Mfg Company, Inc.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K864325. 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 DR7700 OPERATING TABLE?

DR7700 OPERATING TABLE is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Koken Mfg Company, Inc.. The 510(k) number is K864325.

When did DR7700 OPERATING TABLE receive FDA 510(k) clearance?

DR7700 OPERATING TABLE received FDA 510(k) clearance on 1986-11-19, under 510(k) number K864325.

Who is the listed applicant for DR7700 OPERATING TABLE?

The FDA 510(k) record lists Koken Mfg Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR7700 OPERATING TABLE?

The FDA product code for DR7700 OPERATING TABLE is FQO.

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.

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Other records listing Koken Mfg Company, Inc. 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.

K864501KOKEN'S NEW MODEL M-3000 POWER TABLEK864574MAC 150E OPTHALMIC CHAIRK864494MODEL 6500 OPTHALMIC CHAIRK864295DR.500O OPERATING TABLE

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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