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FDA 510(k)

BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70)

K-Number: K971616 · 1998-11-04

ApplicantData Sciences Intl., Inc.
Decision Date1998-11-04
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70) is the device name listed in this FDA 510(k) record. The listed applicant is Data Sciences Intl., Inc.. It received FDA 510(k) clearance on 1998-11-04 under 510(k) number K971616. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70)?

BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70) is a medical device that received FDA 510(k) clearance on 1998-11-04. The listed applicant is Data Sciences Intl., Inc.. The 510(k) number is K971616.

When did BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70) receive FDA 510(k) clearance?

BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70) received FDA 510(k) clearance on 1998-11-04, under 510(k) number K971616.

Who is the listed applicant for BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70)?

The FDA 510(k) record lists Data Sciences Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70)?

The FDA product code for BLOOD PRESSURE MEASUREMENT SYSTEM(DSPM-70) is DQO.

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Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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