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FDA 510(k)

AMP PORTABLE PATIENT PRESSURE MONITOR

K-Number: K802600 · 1980-11-12

ApplicantAmerican Medical Products, Inc.
Decision Date1980-11-12
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMP PORTABLE PATIENT PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Products, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802600. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMP PORTABLE PATIENT PRESSURE MONITOR?

AMP PORTABLE PATIENT PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is American Medical Products, Inc.. The 510(k) number is K802600.

When did AMP PORTABLE PATIENT PRESSURE MONITOR receive FDA 510(k) clearance?

AMP PORTABLE PATIENT PRESSURE MONITOR received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802600.

Who is the listed applicant for AMP PORTABLE PATIENT PRESSURE MONITOR?

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

What is the FDA product code for AMP PORTABLE PATIENT PRESSURE MONITOR?

The FDA product code for AMP PORTABLE PATIENT PRESSURE MONITOR is DSK.

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Other records listing American Medical Products, Inc. as applicant

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Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, Inc.

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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