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FDA 510(k)

NIVP3 (WINDOWS VERSION OF NIVP

K-Number: K970570 · 1997-10-03

ApplicantD. E. Hokanson, Inc.
Decision Date1997-10-03
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NIVP3 (WINDOWS VERSION OF NIVP 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 1997-10-03 under 510(k) number K970570. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIVP3 (WINDOWS VERSION OF NIVP?

NIVP3 (WINDOWS VERSION OF NIVP is a medical device that received FDA 510(k) clearance on 1997-10-03. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K970570.

When did NIVP3 (WINDOWS VERSION OF NIVP receive FDA 510(k) clearance?

NIVP3 (WINDOWS VERSION OF NIVP received FDA 510(k) clearance on 1997-10-03, under 510(k) number K970570.

Who is the listed applicant for NIVP3 (WINDOWS VERSION OF NIVP?

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 NIVP3 (WINDOWS VERSION OF NIVP?

The FDA product code for NIVP3 (WINDOWS VERSION OF NIVP is DQK.

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Other records listing D. E. Hokanson, 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.

K041689POLYURETHANE BLOOD PRESSURE CUFFSK033156OB1 OBSTETRICAL DOPPLERK023707A16 BLOOD FLOW MEASUREMENT SYSTEMK982707EC6 PLETHYSMOGRAPHK973426ANS 2000 ECG MONITOR AND RESPIRATION PACERK932852NON INVASIVE VASCULAR PROGRAM

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Related Devices (Code: DQK)

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K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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