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FDA 510(k)

ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM

K-Number: K981398 · 1998-06-01

ApplicantInterneuron Pharmaceuticals, Inc.
Decision Date1998-06-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Interneuron Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1998-06-01 under 510(k) number K981398. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM?

ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM is a medical device that received FDA 510(k) clearance on 1998-06-01. The listed applicant is Interneuron Pharmaceuticals, Inc.. The 510(k) number is K981398.

When did ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM receive FDA 510(k) clearance?

ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM received FDA 510(k) clearance on 1998-06-01, under 510(k) number K981398.

Who is the listed applicant for ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM?

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

What is the FDA product code for ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM?

The FDA product code for ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM is LNH.

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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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