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FDA 510(k)

SIEMENS CARDIOSTAT 701

K-Number: K790794 · 1979-05-31

ApplicantElmed, Inc.
Decision Date1979-05-31
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS CARDIOSTAT 701 is the device name listed in this FDA 510(k) record. The listed applicant is Elmed, Inc.. It received FDA 510(k) clearance on 1979-05-31 under 510(k) number K790794. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS CARDIOSTAT 701?

SIEMENS CARDIOSTAT 701 is a medical device that received FDA 510(k) clearance on 1979-05-31. The listed applicant is Elmed, Inc.. The 510(k) number is K790794.

When did SIEMENS CARDIOSTAT 701 receive FDA 510(k) clearance?

SIEMENS CARDIOSTAT 701 received FDA 510(k) clearance on 1979-05-31, under 510(k) number K790794.

Who is the listed applicant for SIEMENS CARDIOSTAT 701?

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

What is the FDA product code for SIEMENS CARDIOSTAT 701?

The FDA product code for SIEMENS CARDIOSTAT 701 is DPS.

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Other records listing Elmed, 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.

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Related Devices (Code: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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