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FDA 510(k)

EC 5R PLETHYSMOGRAPH

K-Number: K932812 · 1994-01-13

ApplicantD. E. Hokanson, Inc.
Decision Date1994-01-13
Product CodeJEH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EC 5R 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 1994-01-13 under 510(k) number K932812. The device is classified under product code JEH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EC 5R PLETHYSMOGRAPH?

EC 5R PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1994-01-13. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K932812.

When did EC 5R PLETHYSMOGRAPH receive FDA 510(k) clearance?

EC 5R PLETHYSMOGRAPH received FDA 510(k) clearance on 1994-01-13, under 510(k) number K932812.

Who is the listed applicant for EC 5R 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 EC 5R PLETHYSMOGRAPH?

The FDA product code for EC 5R PLETHYSMOGRAPH is JEH.

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Other records listing D. E. Hokanson, Inc. as applicant

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K041689POLYURETHANE BLOOD PRESSURE CUFFSK033156OB1 OBSTETRICAL DOPPLERK023707A16 BLOOD FLOW MEASUREMENT SYSTEMK982707EC6 PLETHYSMOGRAPHK973426ANS 2000 ECG MONITOR AND RESPIRATION PACERK970570NIVP3 (WINDOWS VERSION OF NIVP

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Related Devices (Code: JEH)

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.

K240706PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)Ganshorn Medizin Electronic GmbHK223818Model 9160 VitaloQUBVitalograph Ireland, Ltd.K072061MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODYViasys Healthcare GmbHK022636BODY BOX 5500Morgan Scientific, Inc.K960840C.E. VASCULAR MACHINEC.E. Diagnosis, Inc.K953642AP-18Jeneric/Pentron, Inc.

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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