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FDA 510(k)

DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY

K-Number: K851973 · 1985-07-26

ApplicantDiasonics, Inc.
Decision Date1985-07-26
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1985-07-26 under 510(k) number K851973. 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 DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY?

DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY is a medical device that received FDA 510(k) clearance on 1985-07-26. The listed applicant is Diasonics, Inc.. The 510(k) number is K851973.

When did DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY receive FDA 510(k) clearance?

DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY received FDA 510(k) clearance on 1985-07-26, under 510(k) number K851973.

Who is the listed applicant for DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY?

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

What is the FDA product code for DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY?

The FDA product code for DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY is 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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