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FDA 510(k)

EC6 PLETHYSMOGRAPH

K-Number: K982707 · 1998-08-26

ApplicantD. E. Hokanson, Inc.
Decision Date1998-08-26
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EC6 PLETHYSMOGRAPH 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 1998-08-26 under 510(k) number K982707. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EC6 PLETHYSMOGRAPH?

EC6 PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1998-08-26. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K982707.

When did EC6 PLETHYSMOGRAPH receive FDA 510(k) clearance?

EC6 PLETHYSMOGRAPH received FDA 510(k) clearance on 1998-08-26, under 510(k) number K982707.

Who is the listed applicant for EC6 PLETHYSMOGRAPH?

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 EC6 PLETHYSMOGRAPH?

The FDA product code for EC6 PLETHYSMOGRAPH is JOM.

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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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