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FDA 510(k)

PICIS CHART+

K-Number: K950536 · 1995-05-17

ApplicantPicis
Decision Date1995-05-17
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PICIS CHART+ is the device name listed in this FDA 510(k) record. The listed applicant is Picis. It received FDA 510(k) clearance on 1995-05-17 under 510(k) number K950536. 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 PICIS CHART+?

PICIS CHART+ is a medical device that received FDA 510(k) clearance on 1995-05-17. The listed applicant is Picis. The 510(k) number is K950536.

When did PICIS CHART+ receive FDA 510(k) clearance?

PICIS CHART+ received FDA 510(k) clearance on 1995-05-17, under 510(k) number K950536.

Who is the listed applicant for PICIS CHART+?

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

What is the FDA product code for PICIS CHART+?

The FDA product code for PICIS CHART+ is MHX.

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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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