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FDA 510(k)

DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE

K-Number: K837085 · 1983-05-09

ApplicantE.M. Adams
Decision Date1983-05-09
Product Code
DecisionSubstantially Equivalent

Device Summary

DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K837085. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE?

DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is E.M. Adams. The 510(k) number is K837085.

When did DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE receive FDA 510(k) clearance?

DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE received FDA 510(k) clearance on 1983-05-09, under 510(k) number K837085.

Who is the listed applicant for DOPPLER FOR DETECTING OCCLUSIONS AND TAKING SYSTOLIC BLOOD PRESSURE?

The FDA 510(k) record lists E.M. Adams as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing E.M. Adams 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.

K905173SPLASH GUARDK910468STERILE DISPOSABLE DRAPE(S)K873978DISPOSABLE BIPOLAR FORCEPSK850063INSTRUMENT POCKETK843724I.V. START KIT & OBSTETRICAL KITK843783WET PACK

View all 21 devices →

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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