Cleared Traditional

K913697 - AUTOMATIC CORNEAL SHAPER

K913697 is an FDA 510(k) clearance for AUTOMATIC CORNEAL SHAPER, manufactured by Hansa Research & Development, Inc.. The device is a Class 1 Ophthalmic device with product code HNO cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K913697 · Hansa Research & Development, Inc. · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1991
Decision
78d
Days
Class 1
Risk

K913697 is an FDA 510(k) clearance for the AUTOMATIC CORNEAL SHAPER. Classified as Keratome, Ac-powered (product code HNO), Class I - General Controls.

Submitted by Hansa Research & Development, Inc. (Miami, US). The FDA issued a Cleared decision on November 5, 1991 after a review of 78 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 Hansa Research & Development, Inc. devices

FDA 510(k) Submission Details - K913697

510(k) Number K913697 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 19, 1991
Decision Date November 05, 1991
Days to Decision 78 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 110d · This submission: 78d
Pathway characteristics
Predicate-based equivalence.

HNO Device Classification - Class 1, General Controls

Product Code HNO Keratome, Ac-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 - HNO Keratome, Ac-powered

All 60
Devices cleared under the same product code (HNO) and FDA review panel - the closest regulatory comparables to K913697.
ML MICROKERATOME BLADE
K962661 · Med-Logics, Inc. · Dec 1996
PLANCON MIRCOLAMELLAR KERATOME
K960395 · Plancon Instruments · Apr 1996
AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT
K941550 · Chiron Vision Corp. · Nov 1994
QUALITATIVE KERATOMETER M823 WITH POWER SUPPLY
K911062 · Storz Instrument Co. · May 1991
STORZ DRAEGER ROTOR KERATOME
K904845 · Storz Instrument Co. · Jan 1991
BKS-1000 REFRACTIVE SET USE IN KERATOREFRACTIVE
K870807 · Allergan, Inc. · May 1987