Cleared Special

K091068 - ACCUTORR V MONITOR

K091068 is the FDA 510(k) clearance for ACCUTORR V MONITOR by Datascope Corp., Patient Monitoring Division. It is a Class 2 Cardiovascular device (product code DXN) cleared through the Special 510(k) pathway after a 24-day FDA review.

K091068 · Datascope Corp., Patient Monitoring Division · Cardiovascular device
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Optimized for regulatory review, auditing and printing
May 2009
Decision
24d
Days
Class 2
Risk

K091068 is an FDA 510(k) clearance for the ACCUTORR V MONITOR, MODEL 0998-00-2000. Classified as System, Measurement, Blood-pressure, Non-invasive (product code DXN), Class II - Special Controls.

Submitted by Datascope Corp., Patient Monitoring Division (Mahwh, US). The FDA issued a Cleared decision on May 8, 2009 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1130 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Datascope Corp., Patient Monitoring Division devices

Submission Details

510(k) Number K091068 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 14, 2009
Decision Date May 08, 2009
Days to Decision 24 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 125d · This submission: 24d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code DXN System, Measurement, Blood-pressure, Non-invasive
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1130
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DXN System, Measurement, Blood-pressure, Non-invasive

All 493
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