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FDA 510(k)

ESCORT PORTABLE PATIENT MONITOR

K-Number: K872291 · 1987-09-25

ApplicantMedical Data Electronics
Decision Date1987-09-25
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ESCORT PORTABLE PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Data Electronics. It received FDA 510(k) clearance on 1987-09-25 under 510(k) number K872291. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESCORT PORTABLE PATIENT MONITOR?

ESCORT PORTABLE PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1987-09-25. The listed applicant is Medical Data Electronics. The 510(k) number is K872291.

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

ESCORT PORTABLE PATIENT MONITOR received FDA 510(k) clearance on 1987-09-25, under 510(k) number K872291.

Who is the listed applicant for ESCORT PORTABLE PATIENT MONITOR?

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

What is the FDA product code for ESCORT PORTABLE PATIENT MONITOR?

The FDA product code for ESCORT PORTABLE PATIENT MONITOR is DXO.

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.

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Other records listing Medical Data Electronics 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.

K014294MODIFICATION TO ESCORT II+ 400 SERIES 9ESCORT PRISM) MONITOR, MODELS 20400, 20401, 20403, 20411, 20412, 20413, 20414K012336MODIFICATION TO:ESCORT VISION CENTRAL STATION TELEMETRY SYSTEM, MODEL 20500K000660ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413K992413ESCORT 100/300 SERIES B (ESCORT II) PATIENT MONITORK992411ESCORT II+ 400 SERIES (ESCORT PRISM) MONITORK982104ESCORT-LINK CENTRAL STATION MONITOR MODEL 20500

View all 27 devices →

Related Devices (Code: DXO)

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.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, 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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