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FDA 510(k)

MODEL 700 PATIENT MONITOR

K-Number: K882118 · 1988-08-02

ApplicantIvy Biomedical Systems, Inc.
Decision Date1988-08-02
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 700 PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ivy Biomedical Systems, Inc.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K882118. 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 MODEL 700 PATIENT MONITOR?

MODEL 700 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Ivy Biomedical Systems, Inc.. The 510(k) number is K882118.

When did MODEL 700 PATIENT MONITOR receive FDA 510(k) clearance?

MODEL 700 PATIENT MONITOR received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882118.

Who is the listed applicant for MODEL 700 PATIENT MONITOR?

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

What is the FDA product code for MODEL 700 PATIENT MONITOR?

The FDA product code for MODEL 700 PATIENT MONITOR 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.

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