Cleared Traditional

K981032 - PIV SYSTEM

K981032 · Medical Solutions, Inc. · General & Plastic Surgery device
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Sep 1998
Decision
167d
Days
-
Risk

K981032 is an FDA 510(k) clearance for the PIV SYSTEM.

Submitted by Medical Solutions, Inc. (Crofton, US). The FDA issued a Cleared decision on September 2, 1998 after a review of 167 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K981032

510(k) Number K981032 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 1998
Decision Date September 02, 1998
Days to Decision 167 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
52d slower than avg
Panel avg: 115d · This submission: 167d
Pathway characteristics
Predicate-based equivalence.

LDQ Device Classification - Class ,

Product Code LDQ
Device Class -

Regulatory Peers - LDQ

All 60
Devices cleared under the same product code (LDQ) and FDA review panel - the closest regulatory comparables to K981032.
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ACU-HALT
K945374 · Eva-Health USA, Inc. · Aug 1995
K981032 · PIV SYSTEM
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