Cleared Traditional

K802925 - 6-415 FILTER, ELEMENT, 170-C

K802925 is an FDA 510(k) clearance for 6-415 FILTER, manufactured by Lifecare Services, Inc.. The device is a Class 2 Cardiovascular device with product code DSK cleared through the Traditional 510(k) pathway after a 30-day FDA review.

K802925 · Lifecare Services, Inc. · Cardiovascular device
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Dec 1980
Decision
30d
Days
Class 2
Risk

K802925 is an FDA 510(k) clearance for the 6-415 FILTER, ELEMENT, 170-C. Classified as Computer, Blood-pressure (product code DSK), Class II - Special Controls.

Submitted by Lifecare Services, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 19, 1980 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1110 - 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 Lifecare Services, Inc. devices

FDA 510(k) Submission Details - K802925

510(k) Number K802925 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 19, 1980
Decision Date December 19, 1980
Days to Decision 30 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
95d faster than avg
Panel avg: 125d · This submission: 30d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DSK Device Classification - Class 2, Special Controls

Product Code DSK Computer, Blood-pressure
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1110
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 - DSK Computer, Blood-pressure

All 48
Devices cleared under the same product code (DSK) and FDA review panel - the closest regulatory comparables to K802925.
PRESSURE FUNCTION BLOCKS
K810172 · Honeywell, Inc. · Feb 1981
PATIENT MONITOR CM111, 112
K810178 · Honeywell, Inc. · Feb 1981
DUAL TRACE PATIENT MONITOR 116,118,120
K810179 · Honeywell, Inc. · Feb 1981
AMP PORTABLE PATIENT PRESSURE MONITOR
K802600 · American Medical Products, Inc. · Nov 1980
PRESSURE MONITOR, MODEL 1131B
K801110 · American Optical Corp. · May 1980
MODEL 1981 PRESSUROMETER DATA ANALYSIS
K792077 · Del Mar Avionics · Dec 1979