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FDA 510(k)

MEDWATCH 400 CARDIAC CENTRAL NURSES STATION

K-Number: K850135 · 1985-05-16

ApplicantMedwatch Systems, Inc.
Decision Date1985-05-16
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDWATCH 400 CARDIAC CENTRAL NURSES STATION is the device name listed in this FDA 510(k) record. The listed applicant is Medwatch Systems, Inc.. It received FDA 510(k) clearance on 1985-05-16 under 510(k) number K850135. 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 MEDWATCH 400 CARDIAC CENTRAL NURSES STATION?

MEDWATCH 400 CARDIAC CENTRAL NURSES STATION is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Medwatch Systems, Inc.. The 510(k) number is K850135.

When did MEDWATCH 400 CARDIAC CENTRAL NURSES STATION receive FDA 510(k) clearance?

MEDWATCH 400 CARDIAC CENTRAL NURSES STATION received FDA 510(k) clearance on 1985-05-16, under 510(k) number K850135.

Who is the listed applicant for MEDWATCH 400 CARDIAC CENTRAL NURSES STATION?

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

What is the FDA product code for MEDWATCH 400 CARDIAC CENTRAL NURSES STATION?

The FDA product code for MEDWATCH 400 CARDIAC CENTRAL NURSES STATION is DRT.

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Related Devices (Code: DRT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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