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FDA 510(k)

COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE

K-Number: K992721 · 1999-09-10

ApplicantRadionics, Inc.
Decision Date1999-09-10
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 1999-09-10 under 510(k) number K992721. 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 COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE?

COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE is a medical device that received FDA 510(k) clearance on 1999-09-10. The listed applicant is Radionics, Inc.. The 510(k) number is K992721.

When did COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE receive FDA 510(k) clearance?

COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE received FDA 510(k) clearance on 1999-09-10, under 510(k) number K992721.

Who is the listed applicant for COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE?

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

What is the FDA product code for COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE?

The FDA product code for COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE 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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