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FDA 510(k)

NPB-4000

K-Number: K962424 · 1996-12-20

ApplicantAnalogic Corp.
Decision Date1996-12-20
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NPB-4000 is the device name listed in this FDA 510(k) record. The listed applicant is Analogic Corp.. It received FDA 510(k) clearance on 1996-12-20 under 510(k) number K962424. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NPB-4000?

NPB-4000 is a medical device that received FDA 510(k) clearance on 1996-12-20. The listed applicant is Analogic Corp.. The 510(k) number is K962424.

When did NPB-4000 receive FDA 510(k) clearance?

NPB-4000 received FDA 510(k) clearance on 1996-12-20, under 510(k) number K962424.

Who is the listed applicant for NPB-4000?

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

What is the FDA product code for NPB-4000?

The FDA product code for NPB-4000 is MHX.

Other records listing Analogic Corp. as applicant

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Official Source

View on FDA Database →

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

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