Cleared Traditional

K911062 - QUALITATIVE KERATOMETER M823 WITH POWER...

K911062 is an FDA 510(k) clearance for QUALITATIVE KERATOMETER M823 WITH POWER..., manufactured by Storz Instrument Co.. The device is a Class 1 Ophthalmic device with product code HNO cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K911062 · Storz Instrument Co. · Ophthalmic device
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May 1991
Decision
72d
Days
Class 1
Risk

K911062 is an FDA 510(k) clearance for the QUALITATIVE KERATOMETER M823 WITH POWER SUPPLY. Classified as Keratome, Ac-powered (product code HNO), Class I - General Controls.

Submitted by Storz Instrument Co. (St. Louis, US). The FDA issued a Cleared decision on May 22, 1991 after a review of 72 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 Storz Instrument Co. devices

FDA 510(k) Submission Details - K911062

510(k) Number K911062 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1991
Decision Date May 22, 1991
Days to Decision 72 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 110d · This submission: 72d
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 14
Devices cleared under the same product code (HNO) and FDA review panel - the closest regulatory comparables to K911062.
MICROKERATOME, MODEL MK-2000
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K941550 · Chiron Vision Corp. · Nov 1994
STORZ DRAEGER ROTOR KERATOME
K904845 · Storz Instrument Co. · Jan 1991
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K870807 · Allergan, Inc. · May 1987
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K864065 · Allergan, Inc. · Dec 1986