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FDA 510(k)

COHORT BONE BRUSH

K-Number: K942108 · 1994-10-11

ApplicantAdvanced Med/Surg, Inc.
Decision Date1994-10-11
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COHORT BONE BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Med/Surg, Inc.. It received FDA 510(k) clearance on 1994-10-11 under 510(k) number K942108. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COHORT BONE BRUSH?

COHORT BONE BRUSH is a medical device that received FDA 510(k) clearance on 1994-10-11. The listed applicant is Advanced Med/Surg, Inc.. The 510(k) number is K942108.

When did COHORT BONE BRUSH receive FDA 510(k) clearance?

COHORT BONE BRUSH received FDA 510(k) clearance on 1994-10-11, under 510(k) number K942108.

Who is the listed applicant for COHORT BONE BRUSH?

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

What is the FDA product code for COHORT BONE BRUSH?

The FDA product code for COHORT BONE BRUSH is HWE.

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Other records listing Advanced Med/Surg, Inc. as applicant

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Related Devices (Code: HWE)

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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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