Cleared Traditional

K870113 - THERMAL JACKET FOR I.V. FLUID BAGS

K870113 is an FDA 510(k) clearance for THERMAL JACKET FOR I.V. FLUID BAGS, manufactured by Thermal Medical Systems, Inc.. The device is a Class 2 General Hospital device with product code KPE cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K870113 · Thermal Medical Systems, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1987
Decision
44d
Days
Class 2
Risk

K870113 is an FDA 510(k) clearance for the THERMAL JACKET FOR I.V. FLUID BAGS. Classified as Container, I.v. (product code KPE), Class II - Special Controls.

Submitted by Thermal Medical Systems, Inc. (Astoria, US). The FDA issued a Cleared decision on February 25, 1987 after a review of 44 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5025 - the FDA general hospital 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 Thermal Medical Systems, Inc. devices

FDA 510(k) Submission Details - K870113

510(k) Number K870113 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 12, 1987
Decision Date February 25, 1987
Days to Decision 44 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 129d · This submission: 44d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPE Device Classification - Class 2, Special Controls

Product Code KPE Container, I.v.
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5025
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 General Hospital devices follow this clearance model.

Regulatory Peers - KPE Container, I.v.

All 60
Devices cleared under the same product code (KPE) and FDA review panel - the closest regulatory comparables to K870113.
OPTUM(TM) AUTOMATED PATIENT ASSIST DEVICE
K883400 · Abbott Laboratories · Dec 1989
CHURCHILL PARENTERAL NUTRITION BAG - EVA
K870395 · Churchill Corp. · Oct 1987
INFUMIX MIXING CONTAINER
K870052 · Biodynamics Corp. · Feb 1987
NUTRIMIX EMPTY CONTAINER
K860042 · Abbott Laboratories · Apr 1986
VIAL DECANTER
K852893 · Advance Medical Designs, Inc. · Sep 1985
BAG DECANTER
K852777 · Advance Medical Designs, Inc. · Aug 1985