Cleared Traditional

K873991 - LAKE IRRIGATION TRAY

K873991 is an FDA 510(k) clearance for LAKE IRRIGATION TRAY, manufactured by Lake Medical Products, Inc.. The device is a Class 2 General Hospital device with product code FMI cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K873991 · Lake Medical Products, Inc. · General Hospital
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Dec 1987
Decision
90d
Days
Class 2
Risk

K873991 is an FDA 510(k) clearance for the LAKE IRRIGATION TRAY. Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by Lake Medical Products, Inc. (Maryland Heights, US). The FDA issued a Cleared decision on December 30, 1987 after a review of 90 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5570 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Lake Medical Products, Inc. devices

FDA 510(k) Submission Details - K873991

510(k) Number K873991 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 01, 1987
Decision Date December 30, 1987
Days to Decision 90 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
39d faster than avg
Panel avg: 129d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMI Device Classification - Class 2, Special Controls

Product Code FMI Needle, Hypodermic, Single Lumen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5570
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 - FMI Needle, Hypodermic, Single Lumen

All 483
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K873991.
NON-CORING NEEDLES
K883009 · Quinton, Inc. · Oct 1988
VIGGO VASCUPORT NEEDLE
K881758 · Ohmeda Medical · Jun 1988
BLOOD COLLECTING NEEDLE AND HOLDERS
K880892 · Abco Dealers, Inc. · Apr 1988
CHEMO-PORT NON-CORING NEEDLES
K873165 · Hdc Corp. · Dec 1987
HR(TM) NEEDLE AND SYRINGE
K874372 · Icu Medical, Inc. · Nov 1987
BLOOD NEEDLE HOLDER
K873569 · Sage Products, Inc. · Nov 1987