FDA 510(k)

HUDSON CRANINAL BURRS

K-Number: K875224 · 1988-01-28

Decision Date1988-01-28

Product CodeHBE

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

HUDSON CRANINAL BURRS is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med, Inc.. It received FDA 510(k) clearance on 1988-01-28 under 510(k) number K875224. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUDSON CRANINAL BURRS?

HUDSON CRANINAL BURRS is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Tri-Med, Inc.. The 510(k) number is K875224.

When did HUDSON CRANINAL BURRS receive FDA 510(k) clearance?

HUDSON CRANINAL BURRS received FDA 510(k) clearance on 1988-01-28, under 510(k) number K875224.

Who is the listed applicant for HUDSON CRANINAL BURRS?

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

What is the FDA product code for HUDSON CRANINAL BURRS?

The FDA product code for HUDSON CRANINAL BURRS is HBE.

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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.