Cleared Traditional

K905847 - STRATO LIFE PORT II DUAL LUMEN PORT/MODIFICATION

K905847 is an FDA 510(k) clearance for STRATO LIFE PORT II DUAL LUMEN PORT/MOD..., manufactured by Strato Medical Corp.. The device is a Class 2 General Hospital device with product code LJT cleared through the Traditional 510(k) pathway after a 99-day FDA review.

K905847 · Strato Medical Corp. · General Hospital
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Apr 1991
Decision
99d
Days
Class 2
Risk

K905847 is an FDA 510(k) clearance for the STRATO LIFE PORT II DUAL LUMEN PORT/MODIFICATION. Classified as Port & Catheter, Implanted, Subcutaneous, Intravascular (product code LJT), Class II - Special Controls.

Submitted by Strato Medical Corp. (Beverly, US). The FDA issued a Cleared decision on April 5, 1991 after a review of 99 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5965 - 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 Strato Medical Corp. devices

FDA 510(k) Submission Details - K905847

510(k) Number K905847 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 1990
Decision Date April 05, 1991
Days to Decision 99 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
30d faster than avg
Panel avg: 129d · This submission: 99d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LJT Device Classification - Class 2, Special Controls

Product Code LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5965
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 - LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

All 238
Devices cleared under the same product code (LJT) and FDA review panel - the closest regulatory comparables to K905847.
LIFEPORT VASCU ACCESS SYST/PORT INTRO KIT 7015
K911355 · Strato Medical Corp. · Apr 1991
STRATO LOW PROFILE PORT(LPS 1055)/MODIFICATION
K905846 · Strato Medical Corp. · Apr 1991
LIFE PT VASC ACCESS PT W/DETACH CATH(LPS 6013)MODI
K905848 · Strato Medical Corp. · Apr 1991
STRATO PLAST W/PRE-ATTACH CATH(LPS 6015)/MODIFIED
K905851 · Strato Medical Corp. · Apr 1991
STRATO STAND METAL PORTS (LPS 1013/1015)/MODIFIED
K905844 · Strato Medical Corp. · Apr 1991
VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM
K910005 · Med Institute, Inc. · Mar 1991