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FDA 510(k)

KOKEN'S NEW MODEL M-3000 POWER TABLE

K-Number: K864501 · 1986-12-16

ApplicantKoken Mfg Company, Inc.
Decision Date1986-12-16
Product Code
DecisionSubstantially Equivalent

Device Summary

KOKEN'S NEW MODEL M-3000 POWER 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 1986-12-16 under 510(k) number K864501. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOKEN'S NEW MODEL M-3000 POWER TABLE?

KOKEN'S NEW MODEL M-3000 POWER TABLE is a medical device that received FDA 510(k) clearance on 1986-12-16. The listed applicant is Koken Mfg Company, Inc.. The 510(k) number is K864501.

When did KOKEN'S NEW MODEL M-3000 POWER TABLE receive FDA 510(k) clearance?

KOKEN'S NEW MODEL M-3000 POWER TABLE received FDA 510(k) clearance on 1986-12-16, under 510(k) number K864501.

Who is the listed applicant for KOKEN'S NEW MODEL M-3000 POWER TABLE?

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

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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.

K864574MAC 150E OPTHALMIC CHAIRK864494MODEL 6500 OPTHALMIC CHAIRK864325DR7700 OPERATING TABLEK864295DR.500O OPERATING TABLE

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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