Cleared Traditional

K982048 - MPS RESERVOIR BAG

K982048 is an FDA 510(k) clearance for MPS RESERVOIR BAG, manufactured by Medical Product Specialists. The device is a Class 2 General Hospital device with product code KPE cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K982048 · Medical Product Specialists · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1998
Decision
47d
Days
Class 2
Risk

K982048 is an FDA 510(k) clearance for the MPS RESERVOIR BAG. Classified as Container, I.v. (product code KPE), Class II - Special Controls.

Submitted by Medical Product Specialists (Brea, US). The FDA issued a Cleared decision on July 27, 1998 after a review of 47 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 Medical Product Specialists devices

FDA 510(k) Submission Details - K982048

510(k) Number K982048 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 1998
Decision Date July 27, 1998
Days to Decision 47 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
82d faster than avg
Panel avg: 129d · This submission: 47d
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 53
Devices cleared under the same product code (KPE) and FDA review panel - the closest regulatory comparables to K982048.
EVA TPN CONTAINER
K041415 · B.Braun Medical, Inc. · Aug 2004
ALL-IN-ONE TWO CHAMBER CONTAINER 3200 ML, 2000 ML & 1000 ML
K020485 · Baxter Healthcare Corp · Mar 2002
ALL-IN-ONE CONTAINER CAT#'S 2B8114,2B8124, 2B8134, 2B8144, 2B8102, 2B8152, 2B8112, 2B8117M 2B8122, 2B8132, 2B8142, 2B712
K983294 · Baxter Healthcare Corp · Nov 1998
STERI-TAMP
K974180 · Pharmacy, Inc. · Feb 1998
CHARTERMED TPN-EVA BAGS
K973103 · Chartermed, Inc. · Nov 1997
VITALMIX PLUS EMPTY I.V. CONTAINER
K972464 · Pacific Device, Inc. · Nov 1997