FDA 510(k)

HANEL MAVIG MONITOR SUSPENSION SYSTEM

K-Number: K954945 · 1996-01-29

Decision Date1996-01-29

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

HANEL MAVIG MONITOR SUSPENSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is F. Walter Hanel GmbH. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K954945. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANEL MAVIG MONITOR SUSPENSION SYSTEM?

HANEL MAVIG MONITOR SUSPENSION SYSTEM is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is F. Walter Hanel GmbH. The 510(k) number is K954945.

When did HANEL MAVIG MONITOR SUSPENSION SYSTEM receive FDA 510(k) clearance?

HANEL MAVIG MONITOR SUSPENSION SYSTEM received FDA 510(k) clearance on 1996-01-29, under 510(k) number K954945.

Who is the listed applicant for HANEL MAVIG MONITOR SUSPENSION SYSTEM?

The FDA 510(k) record lists F. Walter Hanel GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HANEL MAVIG MONITOR SUSPENSION SYSTEM?

The FDA product code for HANEL MAVIG MONITOR SUSPENSION SYSTEM is JAA.

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Other records listing F. Walter Hanel GmbH as applicant

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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.