Cleared Traditional

K833440 - BLOOD SAFETY MODULE BSM2

K833440 is the FDA 510(k) clearance for BLOOD SAFETY MODULE BSM2 by Hospal Medical Corp.. It is a Class 2 Hematology device (product code KOC) cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K833440 · Hospal Medical Corp. · Hematology device
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Dec 1983
Decision
64d
Days
Class 2
Risk

K833440 is an FDA 510(k) clearance for the BLOOD SAFETY MODULE BSM2. Classified as Accessories, Blood Circuit, Hemodialysis (product code KOC), Class II - Special Controls.

Submitted by Hospal Medical Corp. (Mchenry, US). The FDA issued a Cleared decision on December 8, 1983 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 876.5820 - the FDA hematology device 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 Hospal Medical Corp. devices

Submission Details

510(k) Number K833440 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 05, 1983
Decision Date December 08, 1983
Days to Decision 64 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 113d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KOC Accessories, Blood Circuit, Hemodialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 Hematology devices follow this clearance model.

Regulatory Peers - KOC Accessories, Blood Circuit, Hemodialysis

All 114
Devices cleared under the same product code (KOC) and FDA review panel - the closest regulatory comparables to K833440.
NEGATIVE PRESSURE VENOUS BLOOD LINE
K833906 · Erika, Inc. · Jan 1984
DUAL LUMEN NEEDLE
K833308 · Quinton, Inc. · Dec 1983
ERIKA DI-ALA-KIT-SINGLE DIALYSIS ON/OF
K833252 · Erika, Inc. · Dec 1983
CLIRANS MODEL TAF 15 HOLLOW FIBER
K833503 · Terumo Medical Corp. · Dec 1983
NEPHROSS PRESTO
K832666 · Organon Teknika Corp. · Oct 1983
LUNDIA 10-2-L PARALLEL PLATE HEMODIALY
K832894 · Gambro, Inc. · Oct 1983