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FDA 510(k)

OBT STEREOTACTIC SYSTEM

K-Number: K874693 · 1988-03-11

ApplicantTipal Instruments , Ltd.
Decision Date1988-03-11
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

OBT STEREOTACTIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tipal Instruments , Ltd.. It received FDA 510(k) clearance on 1988-03-11 under 510(k) number K874693. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OBT STEREOTACTIC SYSTEM?

OBT STEREOTACTIC SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-11. The listed applicant is Tipal Instruments , Ltd.. The 510(k) number is K874693.

When did OBT STEREOTACTIC SYSTEM receive FDA 510(k) clearance?

OBT STEREOTACTIC SYSTEM received FDA 510(k) clearance on 1988-03-11, under 510(k) number K874693.

Who is the listed applicant for OBT STEREOTACTIC SYSTEM?

The FDA 510(k) record lists Tipal Instruments , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OBT STEREOTACTIC SYSTEM?

The FDA product code for OBT STEREOTACTIC SYSTEM is HAW.

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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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