Cleared Traditional

K974568 - CHASE ANASTOMOSIS VISUALIZATION DEVICE

K974568 is an FDA 510(k) clearance for CHASE ANASTOMOSIS VISUALIZATION DEVICE, manufactured by Chase Medical, Inc.. The device is a Class 2 General Hospital device with product code FQH cleared through the Traditional 510(k) pathway after a 32-day FDA review.

K974568 · Chase Medical, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1998
Decision
32d
Days
Class 2
Risk

K974568 is an FDA 510(k) clearance for the CHASE ANASTOMOSIS VISUALIZATION DEVICE. Classified as Lavage, Jet (product code FQH), Class II - Special Controls.

Submitted by Chase Medical, Inc. (Richardson, US). The FDA issued a Cleared decision on January 6, 1998 after a review of 32 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5475 - 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 Chase Medical, Inc. devices

FDA 510(k) Submission Details - K974568

510(k) Number K974568 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 05, 1997
Decision Date January 06, 1998
Days to Decision 32 days
Submission Type Traditional
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
97d faster than avg
Panel avg: 129d · This submission: 32d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FQH Device Classification - Class 2, Special Controls

Product Code FQH Lavage, Jet
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5475
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 - FQH Lavage, Jet

All 43
Devices cleared under the same product code (FQH) and FDA review panel - the closest regulatory comparables to K974568.
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K973485 · Dlp, Inc. · Dec 1997
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K972551 · Howmedica Corp. · Oct 1997