FDA 510(k)

PERCEPTOR COMPENSATOR MORSE MANIFOLD

K-Number: K951722 · 1996-03-25

ApplicantNamic

Decision Date1996-03-25

Product CodeDRS

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PERCEPTOR COMPENSATOR MORSE MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Namic. It received FDA 510(k) clearance on 1996-03-25 under 510(k) number K951722. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCEPTOR COMPENSATOR MORSE MANIFOLD?

PERCEPTOR COMPENSATOR MORSE MANIFOLD is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is Namic. The 510(k) number is K951722.

When did PERCEPTOR COMPENSATOR MORSE MANIFOLD receive FDA 510(k) clearance?

PERCEPTOR COMPENSATOR MORSE MANIFOLD received FDA 510(k) clearance on 1996-03-25, under 510(k) number K951722.

Who is the listed applicant for PERCEPTOR COMPENSATOR MORSE MANIFOLD?

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

What is the FDA product code for PERCEPTOR COMPENSATOR MORSE MANIFOLD?

The FDA product code for PERCEPTOR COMPENSATOR MORSE MANIFOLD is DRS.

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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.