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FDA 510(k)

BILATERAL TEMPORAL MANDIBULAR JOINT COIL

K-Number: K930991 · 1993-06-18

Decision Date1993-06-18
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BILATERAL TEMPORAL MANDIBULAR JOINT COIL is the device name listed in this FDA 510(k) record. The listed applicant is Magnetic Research, Inc.. It received FDA 510(k) clearance on 1993-06-18 under 510(k) number K930991. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILATERAL TEMPORAL MANDIBULAR JOINT COIL?

BILATERAL TEMPORAL MANDIBULAR JOINT COIL is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Magnetic Research, Inc.. The 510(k) number is K930991.

When did BILATERAL TEMPORAL MANDIBULAR JOINT COIL receive FDA 510(k) clearance?

BILATERAL TEMPORAL MANDIBULAR JOINT COIL received FDA 510(k) clearance on 1993-06-18, under 510(k) number K930991.

Who is the listed applicant for BILATERAL TEMPORAL MANDIBULAR JOINT 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 BILATERAL TEMPORAL MANDIBULAR JOINT COIL?

The FDA product code for BILATERAL TEMPORAL MANDIBULAR JOINT 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.

View all 9 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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