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FDA 510(k)

PATIENTWATCH (TM)

K-Number: K874571 · 1988-01-29

Decision Date1988-01-29
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENTWATCH (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Technology, Inc.. It received FDA 510(k) clearance on 1988-01-29 under 510(k) number K874571. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENTWATCH (TM)?

PATIENTWATCH (TM) is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Advanced Medical Technology, Inc.. The 510(k) number is K874571.

When did PATIENTWATCH (TM) receive FDA 510(k) clearance?

PATIENTWATCH (TM) received FDA 510(k) clearance on 1988-01-29, under 510(k) number K874571.

Who is the listed applicant for PATIENTWATCH (TM)?

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

What is the FDA product code for PATIENTWATCH (TM)?

The FDA product code for PATIENTWATCH (TM) is DSH.

Related Clinical Trials

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.

Other records listing Advanced Medical Technology, Inc. as applicant

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.

View all 7 devices →

Related Devices (Code: DSH)

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.

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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