Cleared Traditional

K911763 - LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2)

K911763 is an FDA 510(k) clearance for LASERFLO BLOOD PERFUSION MONITOR (MODEL..., manufactured by Vasamedics, LLC. The device is a Class 2 Cardiovascular device with product code DPW cleared through the Traditional 510(k) pathway after a 116-day FDA review.

K911763 · Vasamedics, LLC · Cardiovascular device
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Aug 1991
Decision
116d
Days
Class 2
Risk

K911763 is an FDA 510(k) clearance for the LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2). Classified as Flowmeter, Blood, Cardiovascular (product code DPW), Class II - Special Controls.

Submitted by Vasamedics, LLC (Minneapolis, US). The FDA issued a Cleared decision on August 13, 1991 after a review of 116 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2100 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Vasamedics, LLC devices

FDA 510(k) Submission Details - K911763

510(k) Number K911763 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 19, 1991
Decision Date August 13, 1991
Days to Decision 116 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
9d faster than avg
Panel avg: 125d · This submission: 116d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DPW Device Classification - Class 2, Special Controls

Product Code DPW Flowmeter, Blood, Cardiovascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2100
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 - DPW Flowmeter, Blood, Cardiovascular

All 72
Devices cleared under the same product code (DPW) and FDA review panel - the closest regulatory comparables to K911763.
MS DISPOSABLE RIGID DOPPLER PROBE
K930227 · Meadox Medicals, Div. Boston Scientific Corp. · Sep 1993
CARDIOMETRICS SMARTWIRE(TM)/FLOMAP(R)
K925524 · Cardio Metrics, Inc. · Aug 1993
MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG
K913827 · Hewlett-Packard Co. · Nov 1991
INTERSPEC APOGEE, MODIFICATION
K910049 · Interspec, Inc. · Apr 1991
FLOWIRE AND FLOMAP
K905411 · Cardio Metrics, Inc. · Mar 1991
DOPPLER NEEDLE AND FLOW MONITOR
K903625 · Peripheral Systems Group · Nov 1990