Cleared Traditional

K871908 - IV ADMINISTRATION SET

K871908 is an FDA 510(k) clearance for IV ADMINISTRATION SET, manufactured by Travenol Laboratories, S.A.. The device is a Class 2 General Hospital device with product code BRZ cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K871908 · Travenol Laboratories, S.A. · General Hospital
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Jul 1987
Decision
73d
Days
Class 2
Risk

K871908 is an FDA 510(k) clearance for the IV ADMINISTRATION SET. Classified as Set, Blood Transfusion (product code BRZ), Class II - Special Controls.

Submitted by Travenol Laboratories, S.A. (Round Lake, US). The FDA issued a Cleared decision on July 27, 1987 after a review of 73 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - 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 Travenol Laboratories, S.A. devices

FDA 510(k) Submission Details - K871908

510(k) Number K871908 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 15, 1987
Decision Date July 27, 1987
Days to Decision 73 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 129d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BRZ Device Classification - Class 2, Special Controls

Product Code BRZ Set, Blood Transfusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
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 - BRZ Set, Blood Transfusion

All 14
Devices cleared under the same product code (BRZ) and FDA review panel - the closest regulatory comparables to K871908.
MULTISET
K940055 · Puritas Health Care, Inc. · Apr 1994
BLOOD ADMINISTRATION SET
K920788 · Douglas Medical Products Corp. · Jun 1992
JMS TRANSFUSION SET
K880174 · Jms Co., Ltd. · Feb 1988
CHURCHILL BLOOD ADMINISTRATION SET
K864441 · Churchill Corp. · Jan 1987
VYGON EXCHANGE TRANSFUSION TRAY 275.00
K851477 · Vygon Corp. · May 1985