Cleared Traditional

K900857 - NON STERILE PARENTERAL SUPPLY KIT

K900857 is the FDA 510(k) clearance for NON STERILE PARENTERAL SUPPLY KIT by Intermed, Inc.. It is a Class 2 General Hospital device (product code FMF) cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K900857 · Intermed, Inc. · General Hospital
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May 1990
Decision
88d
Days
Class 2
Risk

K900857 is an FDA 510(k) clearance for the NON STERILE PARENTERAL SUPPLY KIT. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Intermed, Inc. (Sparta, US). The FDA issued a Cleared decision on May 22, 1990 after a review of 88 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5860 - 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 Intermed, Inc. devices

Submission Details

510(k) Number K900857 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received February 23, 1990
Decision Date May 22, 1990
Days to Decision 88 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
41d faster than avg
Panel avg: 129d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FMF Syringe, Piston
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5860
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 - FMF Syringe, Piston

All 254
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