FDA 510(k)

PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS

K-Number: K082959 · 2008-10-10

Decision Date2008-10-10

Product CodeDSA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS is the device name listed in this FDA 510(k) record. The listed applicant is Unimed Medical Supplies, Inc.. It received FDA 510(k) clearance on 2008-10-10 under 510(k) number K082959. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS?

PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS is a medical device that received FDA 510(k) clearance on 2008-10-10. The listed applicant is Unimed Medical Supplies, Inc.. The 510(k) number is K082959.

When did PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS receive FDA 510(k) clearance?

PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS received FDA 510(k) clearance on 2008-10-10, under 510(k) number K082959.

Who is the listed applicant for PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS?

The FDA 510(k) record lists Unimed Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS?

The FDA product code for PATIENT MONITORING CABLES FOR ECG, EKG, SPO2 AND BLOOD PRESSURE MONITORS is DSA.

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Other records listing Unimed Medical Supplies, Inc. as applicant

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Related Devices (Code: DSA)

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.