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FDA 510(k)

MAYFIELD TABLE-ELECTRIC

K-Number: K851021 · 1985-05-21

ApplicantOhio Medical Instrument Co., Inc.
Decision Date1985-05-21
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAYFIELD TABLE-ELECTRIC is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Instrument Co., Inc.. It received FDA 510(k) clearance on 1985-05-21 under 510(k) number K851021. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAYFIELD TABLE-ELECTRIC?

MAYFIELD TABLE-ELECTRIC is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Ohio Medical Instrument Co., Inc.. The 510(k) number is K851021.

When did MAYFIELD TABLE-ELECTRIC receive FDA 510(k) clearance?

MAYFIELD TABLE-ELECTRIC received FDA 510(k) clearance on 1985-05-21, under 510(k) number K851021.

Who is the listed applicant for MAYFIELD TABLE-ELECTRIC?

The FDA 510(k) record lists Ohio Medical Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAYFIELD TABLE-ELECTRIC?

The FDA product code for MAYFIELD TABLE-ELECTRIC is GDC.

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Other records listing Ohio Medical Instrument Co., 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.

K021604MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020K013428MAYFIELD/ACCISS OPERATING ARM SYSTEM AND MAYFIELD/OPTICAL ACCISS SYSTEMK992843THE MAYFIELD / ACCISS SYSTEM WITH WINDOWS NT FOR CRANIAL SURGERY, THE MAYFIELD / OPTICAL ACCISS SYSTEM WITH WINDOWS NT FK991267SPINE APPLICATIONS FOR THE MAYFIELD/ACCISS OPERATING ARM AND OPTICAL ACCISS SYSTEMS MODULE, MAYFIELD/ACCISS SPINE RING AK983282OMI OCCIPITAL CERVICAL LOOP, MODEL A1089K982244MAYFIELD ACCISS OPTICAL SYSTEM

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Related Devices (Code: GDC)

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.

K971390QUANTUM 3080SP SURGICAL TABLESTERIS CorporationK970807MOBILE OPERATING TABLE 1132.01Stierlen-Maquet AGK964273DURA-BOARD ARMBOARDAllen Medical Systems, Inc.K940616SKYTRON ELITE 3500 TABLESkytron, Div. the Kmw Group, Inc.K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.K914758MDT/SHAMPAINE MODEL 4900B SURGICAL TABLEMdt Corp., Inc.

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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