Cleared Traditional

K910441 - FLOSCOPE MICRODOP

K910441 is an FDA 510(k) clearance for FLOSCOPE MICRODOP, manufactured by Advance Medical Device, Inc.. The device is a Class 2 Cardiovascular device with product code DPT cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K910441 · Advance Medical Device, Inc. · Cardiovascular device
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Mar 1991
Decision
49d
Days
Class 2
Risk

K910441 is an FDA 510(k) clearance for the FLOSCOPE MICRODOP. Classified as Probe, Blood-flow, Extravascular (product code DPT), Class II - Special Controls.

Submitted by Advance Medical Device, Inc. (Berlin, US). The FDA issued a Cleared decision on March 21, 1991 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2120 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Advance Medical Device, Inc. devices

FDA 510(k) Submission Details - K910441

510(k) Number K910441 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 31, 1991
Decision Date March 21, 1991
Days to Decision 49 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 125d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DPT Device Classification - Class 2, Special Controls

Product Code DPT Probe, Blood-flow, Extravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2120
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 - DPT Probe, Blood-flow, Extravascular

All 15
Devices cleared under the same product code (DPT) and FDA review panel - the closest regulatory comparables to K910441.
TRILLIUM BIO DISPOSABLE BLOOD FLOW PROBE (MODELS DP38T & FP38P)
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K896435 · Hewlett-Packard Co. · Feb 1990