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FDA 510(k)

PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY

K-Number: K837028 · 1983-03-09

ApplicantOhio Medical Instrument Co., Inc.
Decision Date1983-03-09
Product Code
DecisionSubstantially Equivalent

Device Summary

PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY 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 1983-03-09 under 510(k) number K837028. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY?

PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Ohio Medical Instrument Co., Inc.. The 510(k) number is K837028.

When did PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY receive FDA 510(k) clearance?

PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY received FDA 510(k) clearance on 1983-03-09, under 510(k) number K837028.

Who is the listed applicant for PARKINSON NEUROSURGICAL HEADCLAMP FOR SERIAL ANGIOGRAPHY?

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

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Other records listing Ohio Medical Instrument Co., Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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