Cleared Traditional

K841484 - STERILE O.R. BASIN KIT PRODUCT LINE

K841484 is an FDA 510(k) clearance for STERILE O.R. BASIN KIT PRODUCT LINE, manufactured by Medline Industries, Inc.. The device is a Class 2 General Hospital device with product code FRG cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K841484 · Medline Industries, Inc. · General Hospital
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Jul 1984
Decision
83d
Days
Class 2
Risk

K841484 is an FDA 510(k) clearance for the STERILE O.R. BASIN KIT PRODUCT LINE. Classified as Wrap, Sterilization (product code FRG), Class II - Special Controls.

Submitted by Medline Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 2, 1984 after a review of 83 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6850 - 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 Medline Industries, Inc. devices

FDA 510(k) Submission Details - K841484

510(k) Number K841484 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 10, 1984
Decision Date July 02, 1984
Days to Decision 83 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
46d faster than avg
Panel avg: 129d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRG Device Classification - Class 2, Special Controls

Product Code FRG Wrap, Sterilization
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6850
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 - FRG Wrap, Sterilization

All 226
Devices cleared under the same product code (FRG) and FDA review panel - the closest regulatory comparables to K841484.
O.B. BASIN SET
K843982 · Pro-Lab, Inc. · Oct 1984
SKIN SCRUB TRAY STERILE SKIN SCRUB KIT
K842490 · Biological & Environmental Control Laboratories · Aug 1984
DR. GOULD HAND PACK SUSTOM STERIL
K842405 · Pro-Lab, Inc. · Aug 1984
DRESSING CHANGE TRAY
K841123 · Medcare Products · Apr 1984
VANTAGE E
K841156 · American Sterilizer Co. · Apr 1984
JAKOBI SURG. INSTRUMENTS #2 70/71
K834193 · Imm Enterprises , Ltd. · Feb 1984