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FDA 510(k)

NUMARIS 4VA15A

K-Number: K012202 · 2001-09-27

ApplicantSiemens Medical Corp.
Decision Date2001-09-27
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NUMARIS 4VA15A is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Corp.. It received FDA 510(k) clearance on 2001-09-27 under 510(k) number K012202. 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 NUMARIS 4VA15A?

NUMARIS 4VA15A is a medical device that received FDA 510(k) clearance on 2001-09-27. The listed applicant is Siemens Medical Corp.. The 510(k) number is K012202.

When did NUMARIS 4VA15A receive FDA 510(k) clearance?

NUMARIS 4VA15A received FDA 510(k) clearance on 2001-09-27, under 510(k) number K012202.

Who is the listed applicant for NUMARIS 4VA15A?

The FDA 510(k) record lists Siemens Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUMARIS 4VA15A?

The FDA product code for NUMARIS 4VA15A is LNH.

Related Clinical Trials

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Other records listing Siemens Medical Corp. 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.

K010721AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEMK994231SIEMENS INTEGRATED OPERATING SYSTEM (SIOS)K994316MAGNETOM OPEN VIVA WITH PERMANENT MAGNETK9846343D-ANGIO

Related Devices (Code: LNH)

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Official Source

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