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FDA 510(k)

2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF

K-Number: K861987 · 1987-02-03

ApplicantOhmeda Medical
Decision Date1987-02-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1987-02-03 under 510(k) number K861987. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF?

2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF is a medical device that received FDA 510(k) clearance on 1987-02-03. The listed applicant is Ohmeda Medical. The 510(k) number is K861987.

When did 2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF receive FDA 510(k) clearance?

2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF received FDA 510(k) clearance on 1987-02-03, under 510(k) number K861987.

Who is the listed applicant for 2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF?

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

What is the FDA product code for 2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF?

The FDA product code for 2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF is DXN.

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Other records listing Ohmeda Medical as applicant

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Related Devices (Code: DXN)

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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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