Cleared Abbreviated

K992104 - PARSET, MODEL A10001E

K992104 is an FDA 510(k) clearance for PARSET, manufactured by Rd Medical Mfg., Inc.. The device is a Class 2 General Hospital device with product code FPA cleared through the Abbreviated 510(k) pathway after a 62-day FDA review.

K992104 · Rd Medical Mfg., Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1999
Decision
62d
Days
Class 2
Risk

K992104 is an FDA 510(k) clearance for the PARSET, MODEL A10001E. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Rd Medical Mfg., Inc. (Cuelbra, US). The FDA issued a Cleared decision on August 23, 1999 after a review of 62 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - the FDA general hospital device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Rd Medical Mfg., Inc. devices

FDA 510(k) Submission Details - K992104

510(k) Number K992104 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 22, 1999
Decision Date August 23, 1999
Days to Decision 62 days
Submission Type Abbreviated
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
67d faster than avg
Panel avg: 129d · This submission: 62d
Pathway characteristics
Standards-based clearance path.

FPA Device Classification - Class 2, Special Controls

Product Code FPA Set, Administration, Intravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
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 - FPA Set, Administration, Intravascular

All 761
Devices cleared under the same product code (FPA) and FDA review panel - the closest regulatory comparables to K992104.
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