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FDA 510(k)

STEREOPLAN

K-Number: K946252 · 1995-03-14

ApplicantRadionics Software Applications, Inc.
Decision Date1995-03-14
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STEREOPLAN is the device name listed in this FDA 510(k) record. The listed applicant is Radionics Software Applications, Inc.. It received FDA 510(k) clearance on 1995-03-14 under 510(k) number K946252. 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 STEREOPLAN?

STEREOPLAN is a medical device that received FDA 510(k) clearance on 1995-03-14. The listed applicant is Radionics Software Applications, Inc.. The 510(k) number is K946252.

When did STEREOPLAN receive FDA 510(k) clearance?

STEREOPLAN received FDA 510(k) clearance on 1995-03-14, under 510(k) number K946252.

Who is the listed applicant for STEREOPLAN?

The FDA 510(k) record lists Radionics Software Applications, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEREOPLAN?

The FDA product code for STEREOPLAN is HAW.

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Other records listing Radionics Software Applications, Inc. as applicant

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Related Devices (Code: HAW)

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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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