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FDA 510(k)

OB1 OBSTETRICAL DOPPLER

K-Number: K033156 · 2003-12-09

ApplicantD. E. Hokanson, Inc.
Decision Date2003-12-09
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OB1 OBSTETRICAL DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is D. E. Hokanson, Inc.. It received FDA 510(k) clearance on 2003-12-09 under 510(k) number K033156. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OB1 OBSTETRICAL DOPPLER?

OB1 OBSTETRICAL DOPPLER is a medical device that received FDA 510(k) clearance on 2003-12-09. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K033156.

When did OB1 OBSTETRICAL DOPPLER receive FDA 510(k) clearance?

OB1 OBSTETRICAL DOPPLER received FDA 510(k) clearance on 2003-12-09, under 510(k) number K033156.

Who is the listed applicant for OB1 OBSTETRICAL DOPPLER?

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

What is the FDA product code for OB1 OBSTETRICAL DOPPLER?

The FDA product code for OB1 OBSTETRICAL DOPPLER is KNG.

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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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