Cleared Traditional

K904608 - PERCUTANEOUS INTRODUCER TRAY

K904608 is an FDA 510(k) clearance for PERCUTANEOUS INTRODUCER TRAY, manufactured by Thomas Medical Products, Inc.. The device is a Class 2 Cardiovascular device with product code DQY cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K904608 · Thomas Medical Products, Inc. · Cardiovascular device
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Dec 1990
Decision
53d
Days
Class 2
Risk

K904608 is an FDA 510(k) clearance for the PERCUTANEOUS INTRODUCER TRAY. Classified as Catheter, Percutaneous (product code DQY), Class II - Special Controls.

Submitted by Thomas Medical Products, Inc. (Malvern, US). The FDA issued a Cleared decision on December 3, 1990 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1250 - the FDA cardiovascular device oversight 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 Thomas Medical Products, Inc. devices

FDA 510(k) Submission Details - K904608

510(k) Number K904608 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 11, 1990
Decision Date December 03, 1990
Days to Decision 53 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 125d · This submission: 53d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQY Device Classification - Class 2, Special Controls

Product Code DQY Catheter, Percutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1250
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DQY Catheter, Percutaneous

All 707
Devices cleared under the same product code (DQY) and FDA review panel - the closest regulatory comparables to K904608.
VASCULAR RETRIEVAL FORCEPS
K902999 · Cook, Inc. · Feb 1991
ACS URETHAN CORONARY GUIDING CATHETER
K904884 · Advanced Cardiovascular Systems, Inc. · Jan 1991
SCHNEIDER MONORAIL-GEX(TM) GUIDEWIRE EXCHANGE CATH
K902587 · Schneider Intl., Ltd. · Dec 1990
MALLINCKRODT MEDICAL, INC., INFUSSION CATHERTER
K903330 · Mallinckrodt Medical · Oct 1990
THE GUIDER CORONARY GUIDING CATHETER
K903216 · Intec Medical, Inc. · Oct 1990
TAPERED TIP THE GUIDER CORONARY GUIDING CATHETER
K903217 · Intec Medical, Inc. · Oct 1990