Cleared Traditional

K884624 - MVL/MODULAB WITH PVR MODULE

K884624 is an FDA 510(k) clearance for MVL/MODULAB WITH PVR MODULE, manufactured by Life Sciences Manufacturing, Inc.. The device is a Class 2 Cardiovascular device with product code JOM cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K884624 · Life Sciences Manufacturing, Inc. · Cardiovascular device
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Feb 1989
Decision
89d
Days
Class 2
Risk

K884624 is an FDA 510(k) clearance for the MVL/MODULAB WITH PVR MODULE. Classified as Plethysmograph, Photoelectric, Pneumatic Or Hydraulic (product code JOM), Class II - Special Controls.

Submitted by Life Sciences Manufacturing, Inc. (West Lebanon, US). The FDA issued a Cleared decision on February 1, 1989 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2780 - 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 Life Sciences Manufacturing, Inc. devices

FDA 510(k) Submission Details - K884624

510(k) Number K884624 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 04, 1988
Decision Date February 01, 1989
Days to Decision 89 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d faster than avg
Panel avg: 125d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JOM Device Classification - Class 2, Special Controls

Product Code JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2780
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 - JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

All 34
Devices cleared under the same product code (JOM) and FDA review panel - the closest regulatory comparables to K884624.
VENOMETER
K983900 · Advanced Medical Technology , Ltd. · Jan 1999
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K982707 · D. E. Hokanson, Inc. · Aug 1998
VASOCOR PVR 100
K973659 · Vasocor, Inc. · Dec 1997
DOPCORD PPG
K884451 · Huntleigh Technology, Inc. · Jan 1989
3D VASCULAR RECORDER
K883908 · D. E. Hokanson, Inc. · Oct 1988
TL 400 TOTALAB VASCULAR DIAGNOSTIC SYSTEM
K872517 · D. E. Hokanson, Inc. · Oct 1987