ANTERIOR NECK CONTOUR COIL
K-Number: K905512 · 1991-03-07
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Device Summary
Frequently Asked Questions
What is the ANTERIOR NECK CONTOUR COIL?
ANTERIOR NECK CONTOUR COIL is a medical device that received FDA 510(k) clearance on 1991-03-07. The listed applicant is Magnetic Research, Inc.. The 510(k) number is K905512.
When did ANTERIOR NECK CONTOUR COIL receive FDA 510(k) clearance?
ANTERIOR NECK CONTOUR COIL received FDA 510(k) clearance on 1991-03-07, under 510(k) number K905512.
Who is the listed applicant for ANTERIOR NECK CONTOUR COIL?
The FDA 510(k) record lists Magnetic Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANTERIOR NECK CONTOUR COIL?
The FDA product code for ANTERIOR NECK CONTOUR COIL is LNH.
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 Magnetic Research, 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: LNH)
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.
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