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FDA 510(k)

DYNAMOMETER - MODEL FCE AND MODEL MSC

K-Number: K042889 · 2004-11-16

ApplicantAmetek
Decision Date2004-11-16
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DYNAMOMETER - MODEL FCE AND MODEL MSC is the device name listed in this FDA 510(k) record. The listed applicant is Ametek. It received FDA 510(k) clearance on 2004-11-16 under 510(k) number K042889. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNAMOMETER - MODEL FCE AND MODEL MSC?

DYNAMOMETER - MODEL FCE AND MODEL MSC is a medical device that received FDA 510(k) clearance on 2004-11-16. The listed applicant is Ametek. The 510(k) number is K042889.

When did DYNAMOMETER - MODEL FCE AND MODEL MSC receive FDA 510(k) clearance?

DYNAMOMETER - MODEL FCE AND MODEL MSC received FDA 510(k) clearance on 2004-11-16, under 510(k) number K042889.

Who is the listed applicant for DYNAMOMETER - MODEL FCE AND MODEL MSC?

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

What is the FDA product code for DYNAMOMETER - MODEL FCE AND MODEL MSC?

The FDA product code for DYNAMOMETER - MODEL FCE AND MODEL MSC is LBB.

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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.

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