FDA 510(k)

MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT.

K-Number: K882352 · 1988-11-02

ApplicantClinical Information Systems, Inc.

Decision Date1988-11-02

Product CodeCCL

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT. is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Information Systems, Inc.. It received FDA 510(k) clearance on 1988-11-02 under 510(k) number K882352. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT.?

MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT. is a medical device that received FDA 510(k) clearance on 1988-11-02. The listed applicant is Clinical Information Systems, Inc.. The 510(k) number is K882352.

When did MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT. receive FDA 510(k) clearance?

MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT. received FDA 510(k) clearance on 1988-11-02, under 510(k) number K882352.

Who is the listed applicant for MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT.?

The FDA 510(k) record lists Clinical Information Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT.?

The FDA product code for MODEL IDS640 PATIENT DATA DISPLAY & STORAGE MONIT. is CCL.

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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.