FDA 510(k)

PATIENT MONITOR MODEL 701

K-Number: K884096 · 1989-02-23

Decision Date1989-02-23

Product CodeDRT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR MODEL 701 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 1989-02-23 under 510(k) number K884096. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITOR MODEL 701?

PATIENT MONITOR MODEL 701 is a medical device that received FDA 510(k) clearance on 1989-02-23. The listed applicant is Ivy Biomedical Systems, Inc.. The 510(k) number is K884096.

When did PATIENT MONITOR MODEL 701 receive FDA 510(k) clearance?

PATIENT MONITOR MODEL 701 received FDA 510(k) clearance on 1989-02-23, under 510(k) number K884096.

Who is the listed applicant for PATIENT MONITOR MODEL 701?

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 PATIENT MONITOR MODEL 701?

The FDA product code for PATIENT MONITOR MODEL 701 is DRT.

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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.