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FDA 510(k)

PATIENT MONITOR MODEL 703

K-Number: K884662 · 1989-02-02

ApplicantIvy Biomedical Systems, Inc.
Decision Date1989-02-02
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR MODEL 703 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 1989-02-02 under 510(k) number K884662. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITOR MODEL 703?

PATIENT MONITOR MODEL 703 is a medical device that received FDA 510(k) clearance on 1989-02-02. The listed applicant is Ivy Biomedical Systems, Inc.. The 510(k) number is K884662.

When did PATIENT MONITOR MODEL 703 receive FDA 510(k) clearance?

PATIENT MONITOR MODEL 703 received FDA 510(k) clearance on 1989-02-02, under 510(k) number K884662.

Who is the listed applicant for PATIENT MONITOR MODEL 703?

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 703?

The FDA product code for PATIENT MONITOR MODEL 703 is DPS.

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Related Devices (Code: DPS)

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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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