Cleared Traditional

K910378 - PRESSURE MONITORING EXTENSION LINE

K910378 is an FDA 510(k) clearance for PRESSURE MONITORING EXTENSION LINE, manufactured by Professional Medical Services. The device is a Class 2 Cardiovascular device with product code DQO cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K910378 · Professional Medical Services · Cardiovascular device
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Apr 1991
Decision
83d
Days
Class 2
Risk

K910378 is an FDA 510(k) clearance for the PRESSURE MONITORING EXTENSION LINE. Classified as Catheter, Intravascular, Diagnostic (product code DQO), Class II - Special Controls.

Submitted by Professional Medical Services (North Salt Lake, US). The FDA issued a Cleared decision on April 22, 1991 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - 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 Professional Medical Services devices

FDA 510(k) Submission Details - K910378

510(k) Number K910378 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 1991
Decision Date April 22, 1991
Days to Decision 83 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 125d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQO Device Classification - Class 2, Special Controls

Product Code DQO Catheter, Intravascular, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1200
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 - DQO Catheter, Intravascular, Diagnostic

All 350
Devices cleared under the same product code (DQO) and FDA review panel - the closest regulatory comparables to K910378.
CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER
K911703 · Cordis Corp. · Jun 1991
BAXTER MARATHON(TM) INTRAVASCULAR RELAY GUID CATH
K911367 · Baxter Healthcare Corp · Jun 1991
SWAN-GANZ(R) HI-SHORE(R) THERMO CATH W/AMC(TM)
K910204 · Baxter Healthcare Corp · Apr 1991
SCHNEIDER MAGNARAIL PROBING CATHETER
K910259 · Schneider Intl., Ltd. · Apr 1991
CVIS INSIGHT IMAGING CATHETER
K904618 · Cardiovascular Imaging Systems, Inc. · Apr 1991
BAXTER MARATHON(R) INTRAVASCULAR GUIDING CATHETERS
K910208 · Baxter Healthcare Corp · Apr 1991