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FDA 510(k)

MEDRAD PHASED ARRAY NEUROVASCULAR COIL

K-Number: K984257 · 1999-01-25

ApplicantMedrad, Inc.
Decision Date1999-01-25
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDRAD PHASED ARRAY NEUROVASCULAR COIL is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1999-01-25 under 510(k) number K984257. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD PHASED ARRAY NEUROVASCULAR COIL?

MEDRAD PHASED ARRAY NEUROVASCULAR COIL is a medical device that received FDA 510(k) clearance on 1999-01-25. The listed applicant is Medrad, Inc.. The 510(k) number is K984257.

When did MEDRAD PHASED ARRAY NEUROVASCULAR COIL receive FDA 510(k) clearance?

MEDRAD PHASED ARRAY NEUROVASCULAR COIL received FDA 510(k) clearance on 1999-01-25, under 510(k) number K984257.

Who is the listed applicant for MEDRAD PHASED ARRAY NEUROVASCULAR COIL?

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

What is the FDA product code for MEDRAD PHASED ARRAY NEUROVASCULAR COIL?

The FDA product code for MEDRAD PHASED ARRAY NEUROVASCULAR COIL is MOS.

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 Medrad, 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 104 devices →

Related Devices (Code: MOS)

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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