CODMAN FIDUCIAL MARKER SYSTEM
K-Number: K953568 · 1996-02-29
Advertisement
Device Summary
Frequently Asked Questions
What is the CODMAN FIDUCIAL MARKER SYSTEM?
CODMAN FIDUCIAL MARKER SYSTEM is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K953568.
When did CODMAN FIDUCIAL MARKER SYSTEM receive FDA 510(k) clearance?
CODMAN FIDUCIAL MARKER SYSTEM received FDA 510(k) clearance on 1996-02-29, under 510(k) number K953568.
Who is the listed applicant for CODMAN FIDUCIAL MARKER SYSTEM?
The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CODMAN FIDUCIAL MARKER SYSTEM?
The FDA product code for CODMAN FIDUCIAL MARKER SYSTEM is HAW.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Codman & Shurtleff, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HAW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.
Advertisement