QQUADRATURE LUMBAR CONTOUR COIL
K-Number: K922006 · 1992-07-29
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Device Summary
Frequently Asked Questions
What is the QQUADRATURE LUMBAR CONTOUR COIL?
QQUADRATURE LUMBAR CONTOUR COIL is a medical device that received FDA 510(k) clearance on 1992-07-29. The listed applicant is Magnetic Research, Inc.. The 510(k) number is K922006.
When did QQUADRATURE LUMBAR CONTOUR COIL receive FDA 510(k) clearance?
QQUADRATURE LUMBAR CONTOUR COIL received FDA 510(k) clearance on 1992-07-29, under 510(k) number K922006.
Who is the listed applicant for QQUADRATURE LUMBAR 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 QQUADRATURE LUMBAR CONTOUR COIL?
The FDA product code for QQUADRATURE LUMBAR 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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