OBSTETRICAL DOPPLER
K-Number: K841805 · 1984-06-19
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Device Summary
Frequently Asked Questions
What is the OBSTETRICAL DOPPLER?
OBSTETRICAL DOPPLER is a medical device that received FDA 510(k) clearance on 1984-06-19. The listed applicant is Epcom Medical Systems, Inc.. The 510(k) number is K841805.
When did OBSTETRICAL DOPPLER receive FDA 510(k) clearance?
OBSTETRICAL DOPPLER received FDA 510(k) clearance on 1984-06-19, under 510(k) number K841805.
Who is the listed applicant for OBSTETRICAL DOPPLER?
The FDA 510(k) record lists Epcom Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OBSTETRICAL DOPPLER?
The FDA product code for OBSTETRICAL DOPPLER is KNG.
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 Epcom Medical Systems, 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.
Related Devices (Code: KNG)
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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