Cleared Traditional

K981741 - CARRIAZO BARRAQUER MICROKERATOME

K981741 is an FDA 510(k) clearance for CARRIAZO BARRAQUER MICROKERATOME, manufactured by Moria, Inc.. The device is a Class 1 Ophthalmic device with product code HMY cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K981741 · Moria, Inc. · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1998
Decision
67d
Days
Class 1
Risk

K981741 is an FDA 510(k) clearance for the CARRIAZO BARRAQUER MICROKERATOME. Classified as Keratome, Battery-powered (product code HMY), Class I - General Controls.

Submitted by Moria, Inc. (Antony, FR). The FDA issued a Cleared decision on July 24, 1998 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4370 - the FDA ophthalmic 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 Moria, Inc. devices

FDA 510(k) Submission Details - K981741

510(k) Number K981741 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 18, 1998
Decision Date July 24, 1998
Days to Decision 67 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 110d · This submission: 67d
Pathway characteristics
Predicate-based equivalence.

HMY Device Classification - Class 1, General Controls

Product Code HMY Keratome, Battery-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4370
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 - HMY Keratome, Battery-powered

Devices cleared under the same product code (HMY) and FDA review panel - the closest regulatory comparables to K981741.
BD K-4000 MICROKERATOME SYSTEM
K023092 · Becton, Dickinson & CO · Oct 2002
BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME
K022637 · Becton, Dickinson & CO · Oct 2002
KERATOME SYSTEM, MODEL K3000
K984537 · Insight Technologies Instruments, LLC · May 1999
KERATOME SYSTEM
K974243 · Insight Technologies Instruments, LLC · Jan 1998
VISI-DRAPE OPHTHALMIC DRAPES
K902857 · Visitec Co. · Jul 1990
OSCILLATING KNIFE AND ACCESSORIES
K781412 · Codman & Shurtleff, Inc. · Oct 1978