Cleared Traditional

I.V. START KITS (K864693) - FDA 510(k) Clearance

K864693 · Salt Creek Medical Technologies · General & Plastic Surgery device
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Dec 1986
Decision
14d
Days
-
Risk

K864693 is an FDA 510(k) clearance for the I.V. START KITS.

Submitted by Salt Creek Medical Technologies (Canfield, US). The FDA issued a Cleared decision on December 16, 1986 after a review of 14 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel. 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 Salt Creek Medical Technologies devices

Submission Details

510(k) Number K864693 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 1986
Decision Date December 16, 1986
Days to Decision 14 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 115d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -