Cleared Traditional

K941319 - THE WUSCOPE SYSTEM

K941319 is an FDA 510(k) clearance for THE WUSCOPE SYSTEM, manufactured by Achi Corp.. The device is a Class 1 Anesthesiology device with product code CCW cleared through the Traditional 510(k) pathway after a 200-day FDA review.

K941319 · Achi Corp. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1994
Decision
200d
Days
Class 1
Risk

K941319 is an FDA 510(k) clearance for the THE WUSCOPE SYSTEM. Classified as Laryngoscope, Rigid (product code CCW), Class I - General Controls.

Submitted by Achi Corp. (Fremont, US). The FDA issued a Cleared decision on October 4, 1994 after a review of 200 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5540 - the FDA anesthesiology and respiratory 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Achi Corp. devices

FDA 510(k) Submission Details - K941319

510(k) Number K941319 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 1994
Decision Date October 04, 1994
Days to Decision 200 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
60d slower than avg
Panel avg: 140d · This submission: 200d
Pathway characteristics
Predicate-based equivalence.

CCW Device Classification - Class 1, General Controls

Product Code CCW Laryngoscope, Rigid
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5540
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - CCW Laryngoscope, Rigid

All 29
Devices cleared under the same product code (CCW) and FDA review panel - the closest regulatory comparables to K941319.
AUGUSTINE INTUBATION GUIDE
K954446 · Augustine Medical, Inc. · Dec 1995
KARL STORZ SUBGLOTTISCOPE, NEONATE AND INFANT, FIBER OPTIC LIGHT CARRIER, SUCTION TUBE
K951804 · KARL STORZ Endoscopy-America, Inc. · Jun 1995
MCINTOSH, MILLER, FOREGGER BABY
K945425 · Rudolf Riester GmbH & Co. KG · Mar 1995
AUGUSTINE FIBEROPTIC LARYNGOSCOPE
K915161 · Augustine Medical, Inc. · May 1992
AUGUSTINE GUIDE KIT
K921166 · Augustine Medical, Inc. · Apr 1992
BAUMAN DISPOSABLE LARYNGOSCOPE BLADES
K905273 · Vital Signs, Inc. · Mar 1992